Canonical Allele Identifier: CA375765944

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140652379C>T (hg19) ; chr9:g.137757927C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137757927C>T , CM000671.2:g.137757927C>T	GRCh38
NC_000009.11:g.140652379C>T , CM000671.1:g.140652379C>T	GRCh37
NC_000009.10:g.139772200C>T	NCBI36
NG_011776.1:g.143936C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1417C>T MANE Select	ENSP00000417980.1:p.Pro473Ser
ENST00000629335.2:c.1417C>T	ENSP00000490056.1:p.Pro473Ser
ENST00000636027.1:c.1303C>T	ENSP00000489961.1:p.Pro435Ser
ENST00000637161.1:c.1324C>T	ENSP00000490328.1:p.Pro442Ser
ENST00000637261.1:c.1457C>T	ENSP00000490815.1:n.1457C>T
ENST00000637977.1:c.1362C>T
ENST00000638071.1:c.1044C>T
ENST00000640639.1:c.586C>T	ENSP00000491823.1:p.Pro196Ser
ENST00000371394.6:c.*1152C>T	ENSP00000485945.1:n.*1152C>T
ENST00000460843.5:c.1417C>T	ENSP00000417980.1:p.Pro473Ser
ENST00000462484.5:c.1417C>T	ENSP00000417328.1:p.Pro473Ser
ENST00000462942.3:c.274C>T	ENSP00000436107.1:p.Pro92Ser
ENST00000465566.2:c.109C>T	ENSP00000486261.1:p.Pro37Ser
ENST00000629808.2:c.510C>T
NM_001145527.1:c.1417C>T	NP_001138999.1:p.Pro473Ser
NM_024757.4:c.1417C>T	NP_079033.4:p.Pro473Ser
XM_005266105.3:c.1408C>T	XP_005266162.1:p.Pro470Ser
XM_005266110.1:c.1324C>T	XP_005266167.1:p.Pro442Ser
XM_006717288.2:c.1399C>T	XP_006717351.1:p.Pro467Ser
XM_011519021.1:c.1426C>T	XP_011517323.1:p.Pro476Ser
XM_011519022.1:c.1423C>T	XP_011517324.1:p.Pro475Ser
XM_011519023.1:c.1405C>T	XP_011517325.1:p.Pro469Ser
XM_011519024.1:c.1348C>T	XP_011517326.1:p.Pro450Ser
XM_011519025.1:c.1324C>T	XP_011517327.1:p.Pro442Ser
XM_011519026.1:c.1426C>T	XP_011517328.1:p.Pro476Ser
XM_011519027.1:c.1426C>T	XP_011517329.1:p.Pro476Ser
XM_011519028.1:c.1426C>T	XP_011517330.1:p.Pro476Ser
XM_011519033.1:c.1405C>T	XP_011517335.1:p.Pro469Ser
NM_001354259.1:c.1324C>T	NP_001341188.1:p.Pro442Ser
NM_001354263.1:c.1396C>T	NP_001341192.1:p.Pro466Ser
NM_001354611.1:c.1417C>T	NP_001341540.1:p.Pro473Ser
NM_001354612.1:c.1324C>T	NP_001341541.1:p.Pro442Ser
XM_005266105.5:c.1408C>T	XP_005266162.1:p.Pro470Ser
XM_011519021.3:c.1426C>T	XP_011517323.1:p.Pro476Ser
XM_011519022.3:c.1423C>T	XP_011517324.1:p.Pro475Ser
XM_011519023.3:c.1405C>T	XP_011517325.1:p.Pro469Ser
XM_017015134.1:c.1402C>T	XP_016870623.1:p.Pro468Ser
XM_017015136.2:c.1318C>T	XP_016870625.1:p.Pro440Ser
XM_017015137.1:c.1303C>T	XP_016870626.1:p.Pro435Ser
XM_017015138.1:c.1303C>T	XP_016870627.1:p.Pro435Ser
XM_024447674.1:c.1246C>T	XP_024303442.1:p.Pro416Ser
XM_024447675.1:c.1324C>T	XP_024303443.1:p.Pro442Ser
XM_024447676.1:c.541C>T	XP_024303444.1:p.Pro181Ser
XM_024447677.1:c.541C>T	XP_024303445.1:p.Pro181Ser
XM_024447678.1:c.1324C>T	XP_024303446.1:p.Pro442Ser
XM_024447679.1:c.1324C>T	XP_024303447.1:p.Pro442Ser
XM_024447680.1:c.1303C>T	XP_024303448.1:p.Pro435Ser
NM_024757.5:c.1417C>T MANE Select	NP_079033.4:p.Pro473Ser
NM_001145527.2:c.1417C>T	NP_001138999.1:p.Pro473Ser
NM_001354259.2:c.1324C>T	NP_001341188.1:p.Pro442Ser
NM_001354263.2:c.1396C>T	NP_001341192.1:p.Pro466Ser
NM_001354611.2:c.1417C>T	NP_001341540.1:p.Pro473Ser
NM_001354612.2:c.1324C>T	NP_001341541.1:p.Pro442Ser