Canonical Allele Identifier: CA2692881774

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137762669-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137762670del , CM000671.2:g.137762670del	GRCh38
NC_000009.11:g.140657122del , CM000671.1:g.140657122del	GRCh37
NC_000009.10:g.139776943del	NCBI36
NG_011776.1:g.148679del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1502-5del MANE Select	ENSP00000417980.1:n.1502-5del
ENST00000629335.2:c.1502-5del	ENSP00000490056.1:n.1502-5del
ENST00000636027.1:c.1388-5del	ENSP00000489961.1:n.1388-5del
ENST00000637161.1:c.1409-5del	ENSP00000490328.1:n.1409-5del
ENST00000637261.1:c.1542-5del	ENSP00000490815.1:n.1542-5del
ENST00000637977.1:c.1447-5del
ENST00000638071.1:c.1129-5del
ENST00000640639.1:c.671-5del	ENSP00000491823.1:n.671-5del
ENST00000371394.6:c.*1237-5del	ENSP00000485945.1:n.*1237-5del
ENST00000460843.5:c.1502-5del	ENSP00000417980.1:n.1502-5del
ENST00000462484.5:c.1502-5del	ENSP00000417328.1:n.1502-5del
ENST00000462942.3:c.359-5del	ENSP00000436107.1:n.359-5del
ENST00000465566.2:c.194-5del	ENSP00000486261.1:n.194-5del
ENST00000629808.2:c.595-5del
NM_001145527.1:c.1502-5del	NP_001138999.1:n.1502-5del
NM_024757.4:c.1502-5del	NP_079033.4:n.1502-5del
XM_005266105.3:c.1493-5del	XP_005266162.1:n.1493-5del
XM_005266110.1:c.1409-5del	XP_005266167.1:n.1409-5del
XM_006717288.2:c.1484-5del	XP_006717351.1:n.1484-5del
XM_011519021.1:c.1511-5del	XP_011517323.1:n.1511-5del
XM_011519022.1:c.1508-5del	XP_011517324.1:n.1508-5del
XM_011519023.1:c.1490-5del	XP_011517325.1:n.1490-5del
XM_011519024.1:c.1433-5del	XP_011517326.1:n.1433-5del
XM_011519025.1:c.1409-5del	XP_011517327.1:n.1409-5del
XM_011519026.1:c.1511-5del	XP_011517328.1:n.1511-5del
XM_011519027.1:c.1511-5del	XP_011517329.1:n.1511-5del
XM_011519028.1:c.1511-5del	XP_011517330.1:n.1511-5del
XM_011519029.1:c.-68-5del	XP_011517331.1:n.-68-5del
XM_011519033.1:c.1490-5del	XP_011517335.1:n.1490-5del
NM_001354259.1:c.1409-5del	NP_001341188.1:n.1409-5del
NM_001354263.1:c.1481-5del	NP_001341192.1:n.1481-5del
NM_001354611.1:c.1502-5del	NP_001341540.1:n.1502-5del
NM_001354612.1:c.1409-5del	NP_001341541.1:n.1409-5del
XM_005266105.5:c.1493-5del	XP_005266162.1:n.1493-5del
XM_011519021.3:c.1511-5del	XP_011517323.1:n.1511-5del
XM_011519022.3:c.1508-5del	XP_011517324.1:n.1508-5del
XM_011519023.3:c.1490-5del	XP_011517325.1:n.1490-5del
XM_011519029.3:c.-68-5del	XP_011517331.1:n.-68-5del
XM_017015134.1:c.1487-5del	XP_016870623.1:n.1487-5del
XM_017015136.2:c.1403-5del	XP_016870625.1:n.1403-5del
XM_017015137.1:c.1388-5del	XP_016870626.1:n.1388-5del
XM_017015138.1:c.1388-5del	XP_016870627.1:n.1388-5del
XM_024447674.1:c.1331-5del	XP_024303442.1:n.1331-5del
XM_024447675.1:c.1409-5del	XP_024303443.1:n.1409-5del
XM_024447676.1:c.626-5del	XP_024303444.1:n.626-5del
XM_024447677.1:c.626-5del	XP_024303445.1:n.626-5del
XM_024447678.1:c.1409-5del	XP_024303446.1:n.1409-5del
XM_024447679.1:c.1409-5del	XP_024303447.1:n.1409-5del
XM_024447680.1:c.1388-5del	XP_024303448.1:n.1388-5del
NM_024757.5:c.1502-5del MANE Select	NP_079033.4:n.1502-5del
NM_001145527.2:c.1502-5del	NP_001138999.1:n.1502-5del
NM_001354259.2:c.1409-5del	NP_001341188.1:n.1409-5del
NM_001354263.2:c.1481-5del	NP_001341192.1:n.1481-5del
NM_001354611.2:c.1502-5del	NP_001341540.1:n.1502-5del
NM_001354612.2:c.1409-5del	NP_001341541.1:n.1409-5del