Canonical Allele Identifier: CA1884685923

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813520C= , CM000671.2:g.137813520C=	GRCh38
NC_000009.11:g.140707972C= , CM000671.1:g.140707972C=	GRCh37
NC_000009.10:g.139827793C=	NCBI36
NG_011776.1:g.199529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3170C= MANE Select	ENSP00000417980.1:p.Thr1057=
ENST00000637161.1:c.3077C=	ENSP00000490328.1:p.Thr1026=
ENST00000637261.1:c.3210C=	ENSP00000490815.1:n.3210C=
ENST00000637891.1:c.1064C=	ENSP00000490907.1:p.Thr355=
ENST00000460843.5:c.3170C=	ENSP00000417980.1:p.Thr1057=
ENST00000462942.3:c.2027C=	ENSP00000436107.1:p.Thr676=
ENST00000483653.1:n.30C=
ENST00000488242.2:n.696C=
NM_024757.4:c.3170C=	NP_079033.4:p.Thr1057=
XM_005266105.3:c.3161C=	XP_005266162.1:p.Thr1054=
XM_005266110.1:c.3077C=	XP_005266167.1:p.Thr1026=
XM_006717288.2:c.3152C=	XP_006717351.1:p.Thr1051=
XM_011519021.1:c.3179C=	XP_011517323.1:p.Thr1060=
XM_011519022.1:c.3176C=	XP_011517324.1:p.Thr1059=
XM_011519023.1:c.3158C=	XP_011517325.1:p.Thr1053=
XM_011519024.1:c.3101C=	XP_011517326.1:p.Thr1034=
XM_011519025.1:c.3077C=	XP_011517327.1:p.Thr1026=
XM_011519026.1:c.3035C=	XP_011517328.1:p.Thr1012=
XM_011519029.1:c.1601C=	XP_011517331.1:p.Thr534=
XM_011519030.1:c.953C=	XP_011517332.1:p.Thr318=
XM_011519031.1:c.740C=	XP_011517333.1:p.Thr247=
XM_011519032.1:c.740C=	XP_011517334.1:p.Thr247=
XM_011519033.1:c.3014C=	XP_011517335.1:p.Thr1005=
NM_001354263.1:c.3149C=	NP_001341192.1:p.Thr1050=
XM_005266105.5:c.3161C=	XP_005266162.1:p.Thr1054=
XM_011519021.3:c.3179C=	XP_011517323.1:p.Thr1060=
XM_011519022.3:c.3176C=	XP_011517324.1:p.Thr1059=
XM_011519023.3:c.3158C=	XP_011517325.1:p.Thr1053=
XM_011519029.3:c.1601C=	XP_011517331.1:p.Thr534=
XM_011519030.3:c.953C=	XP_011517332.1:p.Thr318=
XM_017015134.1:c.3155C=	XP_016870623.1:p.Thr1052=
XM_017015136.2:c.3071C=	XP_016870625.1:p.Thr1024=
XM_017015137.1:c.3056C=	XP_016870626.1:p.Thr1019=
XM_017015138.1:c.3056C=	XP_016870627.1:p.Thr1019=
XM_024447674.1:c.2999C=	XP_024303442.1:p.Thr1000=
XM_024447675.1:c.2933C=	XP_024303443.1:p.Thr978=
XM_024447676.1:c.2294C=	XP_024303444.1:p.Thr765=
XM_024447677.1:c.2294C=	XP_024303445.1:p.Thr765=
XM_024447680.1:c.2912C=	XP_024303448.1:p.Thr971=
NM_024757.5:c.3170C= MANE Select	NP_079033.4:p.Thr1057=
NM_001354263.2:c.3149C=	NP_001341192.1:p.Thr1050=