Canonical Allele Identifier: CA1884656934

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137757545_137757547delinsCTG , CM000671.2:g.137757545_137757547delinsCTG	GRCh38
NC_000009.11:g.140651997_140651999delinsCTG , CM000671.1:g.140651997_140651999delinsCTG	GRCh37
NC_000009.10:g.139771818_139771820delinsCTG	NCBI36
NG_011776.1:g.143554_143556delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1370-335_1370-333delinsCTG MANE Select	ENSP00000417980.1:n.1370-335_1370-333delinsCTG
ENST00000629335.2:c.1370-335_1370-333delinsCTG	ENSP00000490056.1:n.1370-335_1370-333delinsCTG
ENST00000636027.1:c.1256-335_1256-333delinsCTG	ENSP00000489961.1:n.1256-335_1256-333delinsCTG
ENST00000637161.1:c.1277-335_1277-333delinsCTG	ENSP00000490328.1:n.1277-335_1277-333delinsCTG
ENST00000637261.1:c.1410-335_1410-333delinsCTG	ENSP00000490815.1:n.1410-335_1410-333delinsCTG
ENST00000637977.1:c.1315-335_1315-333delinsCTG
ENST00000638071.1:c.997-335_997-333delinsCTG
ENST00000640639.1:c.539-335_539-333delinsCTG	ENSP00000491823.1:n.539-335_539-333delinsCTG
ENST00000371394.6:c.*1105-335_*1105-333delinsCTG	ENSP00000485945.1:n.*1105-335_*1105-333delinsCTG
ENST00000460843.5:c.1370-335_1370-333delinsCTG	ENSP00000417980.1:n.1370-335_1370-333delinsCTG
ENST00000462484.5:c.1370-335_1370-333delinsCTG	ENSP00000417328.1:n.1370-335_1370-333delinsCTG
ENST00000462942.3:c.227-335_227-333delinsCTG	ENSP00000436107.1:n.227-335_227-333delinsCTG
ENST00000465566.2:c.62-335_62-333delinsCTG	ENSP00000486261.1:n.62-335_62-333delinsCTG
ENST00000626066.2:c.1273-335_1273-333delinsCTG
ENST00000629808.2:c.463-335_463-333delinsCTG
NM_001145527.1:c.1370-335_1370-333delinsCTG	NP_001138999.1:n.1370-335_1370-333delinsCTG
NM_024757.4:c.1370-335_1370-333delinsCTG	NP_079033.4:n.1370-335_1370-333delinsCTG
XM_005266105.3:c.1361-335_1361-333delinsCTG	XP_005266162.1:n.1361-335_1361-333delinsCTG
XM_005266110.1:c.1277-335_1277-333delinsCTG	XP_005266167.1:n.1277-335_1277-333delinsCTG
XM_006717288.2:c.1352-335_1352-333delinsCTG	XP_006717351.1:n.1352-335_1352-333delinsCTG
XM_011519021.1:c.1379-335_1379-333delinsCTG	XP_011517323.1:n.1379-335_1379-333delinsCTG
XM_011519022.1:c.1376-335_1376-333delinsCTG	XP_011517324.1:n.1376-335_1376-333delinsCTG
XM_011519023.1:c.1358-335_1358-333delinsCTG	XP_011517325.1:n.1358-335_1358-333delinsCTG
XM_011519024.1:c.1301-335_1301-333delinsCTG	XP_011517326.1:n.1301-335_1301-333delinsCTG
XM_011519025.1:c.1277-335_1277-333delinsCTG	XP_011517327.1:n.1277-335_1277-333delinsCTG
XM_011519026.1:c.1379-335_1379-333delinsCTG	XP_011517328.1:n.1379-335_1379-333delinsCTG
XM_011519027.1:c.1379-335_1379-333delinsCTG	XP_011517329.1:n.1379-335_1379-333delinsCTG
XM_011519028.1:c.1379-335_1379-333delinsCTG	XP_011517330.1:n.1379-335_1379-333delinsCTG
XM_011519033.1:c.1358-335_1358-333delinsCTG	XP_011517335.1:n.1358-335_1358-333delinsCTG
NM_001354259.1:c.1277-335_1277-333delinsCTG	NP_001341188.1:n.1277-335_1277-333delinsCTG
NM_001354263.1:c.1349-335_1349-333delinsCTG	NP_001341192.1:n.1349-335_1349-333delinsCTG
NM_001354611.1:c.1370-335_1370-333delinsCTG	NP_001341540.1:n.1370-335_1370-333delinsCTG
NM_001354612.1:c.1277-335_1277-333delinsCTG	NP_001341541.1:n.1277-335_1277-333delinsCTG
XM_005266105.5:c.1361-335_1361-333delinsCTG	XP_005266162.1:n.1361-335_1361-333delinsCTG
XM_011519021.3:c.1379-335_1379-333delinsCTG	XP_011517323.1:n.1379-335_1379-333delinsCTG
XM_011519022.3:c.1376-335_1376-333delinsCTG	XP_011517324.1:n.1376-335_1376-333delinsCTG
XM_011519023.3:c.1358-335_1358-333delinsCTG	XP_011517325.1:n.1358-335_1358-333delinsCTG
XM_017015134.1:c.1355-335_1355-333delinsCTG	XP_016870623.1:n.1355-335_1355-333delinsCTG
XM_017015136.2:c.1271-335_1271-333delinsCTG	XP_016870625.1:n.1271-335_1271-333delinsCTG
XM_017015137.1:c.1256-335_1256-333delinsCTG	XP_016870626.1:n.1256-335_1256-333delinsCTG
XM_017015138.1:c.1256-335_1256-333delinsCTG	XP_016870627.1:n.1256-335_1256-333delinsCTG
XM_024447674.1:c.1199-335_1199-333delinsCTG	XP_024303442.1:n.1199-335_1199-333delinsCTG
XM_024447675.1:c.1277-335_1277-333delinsCTG	XP_024303443.1:n.1277-335_1277-333delinsCTG
XM_024447676.1:c.494-335_494-333delinsCTG	XP_024303444.1:n.494-335_494-333delinsCTG
XM_024447677.1:c.494-335_494-333delinsCTG	XP_024303445.1:n.494-335_494-333delinsCTG
XM_024447678.1:c.1277-335_1277-333delinsCTG	XP_024303446.1:n.1277-335_1277-333delinsCTG
XM_024447679.1:c.1277-335_1277-333delinsCTG	XP_024303447.1:n.1277-335_1277-333delinsCTG
XM_024447680.1:c.1256-335_1256-333delinsCTG	XP_024303448.1:n.1256-335_1256-333delinsCTG
NM_024757.5:c.1370-335_1370-333delinsCTG MANE Select	NP_079033.4:n.1370-335_1370-333delinsCTG
NM_001145527.2:c.1370-335_1370-333delinsCTG	NP_001138999.1:n.1370-335_1370-333delinsCTG
NM_001354259.2:c.1277-335_1277-333delinsCTG	NP_001341188.1:n.1277-335_1277-333delinsCTG
NM_001354263.2:c.1349-335_1349-333delinsCTG	NP_001341192.1:n.1349-335_1349-333delinsCTG
NM_001354611.2:c.1370-335_1370-333delinsCTG	NP_001341540.1:n.1370-335_1370-333delinsCTG
NM_001354612.2:c.1277-335_1277-333delinsCTG	NP_001341541.1:n.1277-335_1277-333delinsCTG