Canonical Allele Identifier: CA1884659567

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137762716C= , CM000671.2:g.137762716C=	GRCh38
NC_000009.11:g.140657168C= , CM000671.1:g.140657168C=	GRCh37
NC_000009.10:g.139776989C=	NCBI36
NG_011776.1:g.148725C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1543C= MANE Select	ENSP00000417980.1:p.Gln515=
ENST00000629335.2:c.1543C=	ENSP00000490056.1:p.Gln515=
ENST00000636027.1:c.1429C=	ENSP00000489961.1:p.Gln477=
ENST00000637161.1:c.1450C=	ENSP00000490328.1:p.Gln484=
ENST00000637261.1:c.1583C=	ENSP00000490815.1:n.1583C=
ENST00000637977.1:c.1488C=
ENST00000638071.1:c.1170C=
ENST00000640639.1:c.712C=	ENSP00000491823.1:p.Gln238=
ENST00000371394.6:c.*1278C=	ENSP00000485945.1:n.*1278C=
ENST00000460843.5:c.1543C=	ENSP00000417980.1:p.Gln515=
ENST00000462484.5:c.1543C=	ENSP00000417328.1:p.Gln515=
ENST00000462942.3:c.400C=	ENSP00000436107.1:p.Gln134=
ENST00000465566.2:c.235C=	ENSP00000486261.1:p.Gln79=
ENST00000629808.2:c.636C=
NM_001145527.1:c.1543C=	NP_001138999.1:p.Gln515=
NM_024757.4:c.1543C=	NP_079033.4:p.Gln515=
XM_005266105.3:c.1534C=	XP_005266162.1:p.Gln512=
XM_005266110.1:c.1450C=	XP_005266167.1:p.Gln484=
XM_006717288.2:c.1525C=	XP_006717351.1:p.Gln509=
XM_011519021.1:c.1552C=	XP_011517323.1:p.Gln518=
XM_011519022.1:c.1549C=	XP_011517324.1:p.Gln517=
XM_011519023.1:c.1531C=	XP_011517325.1:p.Gln511=
XM_011519024.1:c.1474C=	XP_011517326.1:p.Gln492=
XM_011519025.1:c.1450C=	XP_011517327.1:p.Gln484=
XM_011519026.1:c.1552C=	XP_011517328.1:p.Gln518=
XM_011519027.1:c.1552C=	XP_011517329.1:p.Gln518=
XM_011519028.1:c.1552C=	XP_011517330.1:p.Gln518=
XM_011519029.1:c.-27C=	XP_011517331.1:n.-27C=
XM_011519033.1:c.1531C=	XP_011517335.1:p.Gln511=
NM_001354259.1:c.1450C=	NP_001341188.1:p.Gln484=
NM_001354263.1:c.1522C=	NP_001341192.1:p.Gln508=
NM_001354611.1:c.1543C=	NP_001341540.1:p.Gln515=
NM_001354612.1:c.1450C=	NP_001341541.1:p.Gln484=
XM_005266105.5:c.1534C=	XP_005266162.1:p.Gln512=
XM_011519021.3:c.1552C=	XP_011517323.1:p.Gln518=
XM_011519022.3:c.1549C=	XP_011517324.1:p.Gln517=
XM_011519023.3:c.1531C=	XP_011517325.1:p.Gln511=
XM_011519029.3:c.-27C=	XP_011517331.1:n.-27C=
XM_017015134.1:c.1528C=	XP_016870623.1:p.Gln510=
XM_017015136.2:c.1444C=	XP_016870625.1:p.Gln482=
XM_017015137.1:c.1429C=	XP_016870626.1:p.Gln477=
XM_017015138.1:c.1429C=	XP_016870627.1:p.Gln477=
XM_024447674.1:c.1372C=	XP_024303442.1:p.Gln458=
XM_024447675.1:c.1450C=	XP_024303443.1:p.Gln484=
XM_024447676.1:c.667C=	XP_024303444.1:p.Gln223=
XM_024447677.1:c.667C=	XP_024303445.1:p.Gln223=
XM_024447678.1:c.1450C=	XP_024303446.1:p.Gln484=
XM_024447679.1:c.1450C=	XP_024303447.1:p.Gln484=
XM_024447680.1:c.1429C=	XP_024303448.1:p.Gln477=
NM_024757.5:c.1543C= MANE Select	NP_079033.4:p.Gln515=
NM_001145527.2:c.1543C=	NP_001138999.1:p.Gln515=
NM_001354259.2:c.1450C=	NP_001341188.1:p.Gln484=
NM_001354263.2:c.1522C=	NP_001341192.1:p.Gln508=
NM_001354611.2:c.1543C=	NP_001341540.1:p.Gln515=
NM_001354612.2:c.1450C=	NP_001341541.1:p.Gln484=