Canonical Allele Identifier: CA1884685689

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813074C= , CM000671.2:g.137813074C=	GRCh38
NC_000009.11:g.140707526C= , CM000671.1:g.140707526C=	GRCh37
NC_000009.10:g.139827347C=	NCBI36
NG_011776.1:g.199083C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2936C= MANE Select	ENSP00000417980.1:p.Ala979=
ENST00000636027.1:c.2822C=	ENSP00000489961.1:p.Ala941=
ENST00000637161.1:c.2843C=	ENSP00000490328.1:p.Ala948=
ENST00000637261.1:c.2976C=	ENSP00000490815.1:n.2976C=
ENST00000637891.1:c.830C=	ENSP00000490907.1:p.Ala277=
ENST00000460843.5:c.2936C=	ENSP00000417980.1:p.Ala979=
ENST00000462942.3:c.1793C=	ENSP00000436107.1:p.Ala598=
ENST00000486164.5:c.623C=
ENST00000488242.2:n.462C=
NM_024757.4:c.2936C=	NP_079033.4:p.Ala979=
XM_005266105.3:c.2927C=	XP_005266162.1:p.Ala976=
XM_005266110.1:c.2843C=	XP_005266167.1:p.Ala948=
XM_006717288.2:c.2918C=	XP_006717351.1:p.Ala973=
XM_011519021.1:c.2945C=	XP_011517323.1:p.Ala982=
XM_011519022.1:c.2942C=	XP_011517324.1:p.Ala981=
XM_011519023.1:c.2924C=	XP_011517325.1:p.Ala975=
XM_011519024.1:c.2867C=	XP_011517326.1:p.Ala956=
XM_011519025.1:c.2843C=	XP_011517327.1:p.Ala948=
XM_011519026.1:c.2801C=	XP_011517328.1:p.Ala934=
XM_011519029.1:c.1367C=	XP_011517331.1:p.Ala456=
XM_011519030.1:c.719C=	XP_011517332.1:p.Ala240=
XM_011519031.1:c.506C=	XP_011517333.1:p.Ala169=
XM_011519032.1:c.506C=	XP_011517334.1:p.Ala169=
XM_011519033.1:c.2780C=	XP_011517335.1:p.Ala927=
NM_001354263.1:c.2915C=	NP_001341192.1:p.Ala972=
XM_005266105.5:c.2927C=	XP_005266162.1:p.Ala976=
XM_011519021.3:c.2945C=	XP_011517323.1:p.Ala982=
XM_011519022.3:c.2942C=	XP_011517324.1:p.Ala981=
XM_011519023.3:c.2924C=	XP_011517325.1:p.Ala975=
XM_011519029.3:c.1367C=	XP_011517331.1:p.Ala456=
XM_011519030.3:c.719C=	XP_011517332.1:p.Ala240=
XM_017015134.1:c.2921C=	XP_016870623.1:p.Ala974=
XM_017015136.2:c.2837C=	XP_016870625.1:p.Ala946=
XM_017015137.1:c.2822C=	XP_016870626.1:p.Ala941=
XM_017015138.1:c.2822C=	XP_016870627.1:p.Ala941=
XM_024447674.1:c.2765C=	XP_024303442.1:p.Ala922=
XM_024447675.1:c.2699C=	XP_024303443.1:p.Ala900=
XM_024447676.1:c.2060C=	XP_024303444.1:p.Ala687=
XM_024447677.1:c.2060C=	XP_024303445.1:p.Ala687=
XM_024447680.1:c.2678C=	XP_024303448.1:p.Ala893=
NM_024757.5:c.2936C= MANE Select	NP_079033.4:p.Ala979=
NM_001354263.2:c.2915C=	NP_001341192.1:p.Ala972=