Canonical Allele Identifier: CA1884679265

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800892T= , CM000671.2:g.137800892T=	GRCh38
NC_000009.11:g.140695344T= , CM000671.1:g.140695344T=	GRCh37
NC_000009.10:g.139815165T=	NCBI36
NG_011776.1:g.186901T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2620T= MANE Select	ENSP00000417980.1:p.Trp874=
ENST00000636027.1:c.2506T=	ENSP00000489961.1:p.Trp836=
ENST00000637161.1:c.2527T=	ENSP00000490328.1:p.Trp843=
ENST00000637261.1:c.2660T=	ENSP00000490815.1:n.2660T=
ENST00000637891.1:c.514T=	ENSP00000490907.1:p.Trp172=
ENST00000637949.1:c.298T=	ENSP00000489786.1:p.Trp100=
ENST00000460843.5:c.2620T=	ENSP00000417980.1:p.Trp874=
ENST00000462942.3:c.1477T=	ENSP00000436107.1:p.Trp493=
ENST00000482340.5:c.190T=	ENSP00000486748.1:p.Trp64=
ENST00000486164.5:c.198T=
ENST00000488242.2:n.146T=
ENST00000493484.5:c.190T=	ENSP00000486503.1:p.Trp64=
NM_024757.4:c.2620T=	NP_079033.4:p.Trp874=
XM_005266105.3:c.2611T=	XP_005266162.1:p.Trp871=
XM_005266110.1:c.2527T=	XP_005266167.1:p.Trp843=
XM_006717288.2:c.2602T=	XP_006717351.1:p.Trp868=
XM_011519021.1:c.2629T=	XP_011517323.1:p.Trp877=
XM_011519022.1:c.2626T=	XP_011517324.1:p.Trp876=
XM_011519023.1:c.2608T=	XP_011517325.1:p.Trp870=
XM_011519024.1:c.2551T=	XP_011517326.1:p.Trp851=
XM_011519025.1:c.2527T=	XP_011517327.1:p.Trp843=
XM_011519026.1:c.2485T=	XP_011517328.1:p.Trp829=
XM_011519027.1:c.2629T=	XP_011517329.1:p.Trp877=
XM_011519029.1:c.1051T=	XP_011517331.1:p.Trp351=
XM_011519030.1:c.403T=	XP_011517332.1:p.Trp135=
XM_011519031.1:c.190T=	XP_011517333.1:p.Trp64=
XM_011519032.1:c.190T=	XP_011517334.1:p.Trp64=
XM_011519033.1:c.2464T=	XP_011517335.1:p.Trp822=
NM_001354263.1:c.2599T=	NP_001341192.1:p.Trp867=
XM_005266105.5:c.2611T=	XP_005266162.1:p.Trp871=
XM_011519021.3:c.2629T=	XP_011517323.1:p.Trp877=
XM_011519022.3:c.2626T=	XP_011517324.1:p.Trp876=
XM_011519023.3:c.2608T=	XP_011517325.1:p.Trp870=
XM_011519029.3:c.1051T=	XP_011517331.1:p.Trp351=
XM_011519030.3:c.403T=	XP_011517332.1:p.Trp135=
XM_017015134.1:c.2605T=	XP_016870623.1:p.Trp869=
XM_017015136.2:c.2521T=	XP_016870625.1:p.Trp841=
XM_017015137.1:c.2506T=	XP_016870626.1:p.Trp836=
XM_017015138.1:c.2506T=	XP_016870627.1:p.Trp836=
XM_024447674.1:c.2449T=	XP_024303442.1:p.Trp817=
XM_024447675.1:c.2383T=	XP_024303443.1:p.Trp795=
XM_024447676.1:c.1744T=	XP_024303444.1:p.Trp582=
XM_024447677.1:c.1744T=	XP_024303445.1:p.Trp582=
XM_024447678.1:c.2527T=	XP_024303446.1:p.Trp843=
XM_024447680.1:c.2362T=	XP_024303448.1:p.Trp788=
NM_024757.5:c.2620T= MANE Select	NP_079033.4:p.Trp874=
NM_001354263.2:c.2599T=	NP_001341192.1:p.Trp867=