Canonical Allele Identifier: CA1884685729

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813150C= , CM000671.2:g.137813150C=	GRCh38
NC_000009.11:g.140707602C= , CM000671.1:g.140707602C=	GRCh37
NC_000009.10:g.139827423C=	NCBI36
NG_011776.1:g.199159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3012C= MANE Select	ENSP00000417980.1:p.Ser1004=
ENST00000636027.1:c.2898C=	ENSP00000489961.1:p.Ser966=
ENST00000637161.1:c.2919C=	ENSP00000490328.1:p.Ser973=
ENST00000637261.1:c.3052C=	ENSP00000490815.1:n.3052C=
ENST00000637891.1:c.906C=	ENSP00000490907.1:p.Ser302=
ENST00000460843.5:c.3012C=	ENSP00000417980.1:p.Ser1004=
ENST00000462942.3:c.1869C=	ENSP00000436107.1:p.Ser623=
ENST00000486164.5:c.699C=
ENST00000488242.2:n.538C=
NM_024757.4:c.3012C=	NP_079033.4:p.Ser1004=
XM_005266105.3:c.3003C=	XP_005266162.1:p.Ser1001=
XM_005266110.1:c.2919C=	XP_005266167.1:p.Ser973=
XM_006717288.2:c.2994C=	XP_006717351.1:p.Ser998=
XM_011519021.1:c.3021C=	XP_011517323.1:p.Ser1007=
XM_011519022.1:c.3018C=	XP_011517324.1:p.Ser1006=
XM_011519023.1:c.3000C=	XP_011517325.1:p.Ser1000=
XM_011519024.1:c.2943C=	XP_011517326.1:p.Ser981=
XM_011519025.1:c.2919C=	XP_011517327.1:p.Ser973=
XM_011519026.1:c.2877C=	XP_011517328.1:p.Ser959=
XM_011519029.1:c.1443C=	XP_011517331.1:p.Ser481=
XM_011519030.1:c.795C=	XP_011517332.1:p.Ser265=
XM_011519031.1:c.582C=	XP_011517333.1:p.Ser194=
XM_011519032.1:c.582C=	XP_011517334.1:p.Ser194=
XM_011519033.1:c.2856C=	XP_011517335.1:p.Ser952=
NM_001354263.1:c.2991C=	NP_001341192.1:p.Ser997=
XM_005266105.5:c.3003C=	XP_005266162.1:p.Ser1001=
XM_011519021.3:c.3021C=	XP_011517323.1:p.Ser1007=
XM_011519022.3:c.3018C=	XP_011517324.1:p.Ser1006=
XM_011519023.3:c.3000C=	XP_011517325.1:p.Ser1000=
XM_011519029.3:c.1443C=	XP_011517331.1:p.Ser481=
XM_011519030.3:c.795C=	XP_011517332.1:p.Ser265=
XM_017015134.1:c.2997C=	XP_016870623.1:p.Ser999=
XM_017015136.2:c.2913C=	XP_016870625.1:p.Ser971=
XM_017015137.1:c.2898C=	XP_016870626.1:p.Ser966=
XM_017015138.1:c.2898C=	XP_016870627.1:p.Ser966=
XM_024447674.1:c.2841C=	XP_024303442.1:p.Ser947=
XM_024447675.1:c.2775C=	XP_024303443.1:p.Ser925=
XM_024447676.1:c.2136C=	XP_024303444.1:p.Ser712=
XM_024447677.1:c.2136C=	XP_024303445.1:p.Ser712=
XM_024447680.1:c.2754C=	XP_024303448.1:p.Ser918=
NM_024757.5:c.3012C= MANE Select	NP_079033.4:p.Ser1004=
NM_001354263.2:c.2991C=	NP_001341192.1:p.Ser997=