Canonical Allele Identifier: CA375793834

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707851G>C (hg19) ; chr9:g.137813399G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813399G>C , CM000671.2:g.137813399G>C	GRCh38
NC_000009.11:g.140707851G>C , CM000671.1:g.140707851G>C	GRCh37
NC_000009.10:g.139827672G>C	NCBI36
NG_011776.1:g.199408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3049G>C MANE Select	ENSP00000417980.1:p.Gly1017Arg
ENST00000636027.1:c.2935G>C	ENSP00000489961.1:p.Gly979Arg
ENST00000637161.1:c.2956G>C	ENSP00000490328.1:p.Gly986Arg
ENST00000637261.1:c.3089G>C	ENSP00000490815.1:n.3089G>C
ENST00000637891.1:c.943G>C	ENSP00000490907.1:p.Gly315Arg
ENST00000460843.5:c.3049G>C	ENSP00000417980.1:p.Gly1017Arg
ENST00000462942.3:c.1906G>C	ENSP00000436107.1:p.Gly636Arg
ENST00000486164.5:c.736G>C
ENST00000488242.2:n.575G>C
NM_024757.4:c.3049G>C	NP_079033.4:p.Gly1017Arg
XM_005266105.3:c.3040G>C	XP_005266162.1:p.Gly1014Arg
XM_005266110.1:c.2956G>C	XP_005266167.1:p.Gly986Arg
XM_006717288.2:c.3031G>C	XP_006717351.1:p.Gly1011Arg
XM_011519021.1:c.3058G>C	XP_011517323.1:p.Gly1020Arg
XM_011519022.1:c.3055G>C	XP_011517324.1:p.Gly1019Arg
XM_011519023.1:c.3037G>C	XP_011517325.1:p.Gly1013Arg
XM_011519024.1:c.2980G>C	XP_011517326.1:p.Gly994Arg
XM_011519025.1:c.2956G>C	XP_011517327.1:p.Gly986Arg
XM_011519026.1:c.2914G>C	XP_011517328.1:p.Gly972Arg
XM_011519029.1:c.1480G>C	XP_011517331.1:p.Gly494Arg
XM_011519030.1:c.832G>C	XP_011517332.1:p.Gly278Arg
XM_011519031.1:c.619G>C	XP_011517333.1:p.Gly207Arg
XM_011519032.1:c.619G>C	XP_011517334.1:p.Gly207Arg
XM_011519033.1:c.2893G>C	XP_011517335.1:p.Gly965Arg
NM_001354263.1:c.3028G>C	NP_001341192.1:p.Gly1010Arg
XM_005266105.5:c.3040G>C	XP_005266162.1:p.Gly1014Arg
XM_011519021.3:c.3058G>C	XP_011517323.1:p.Gly1020Arg
XM_011519022.3:c.3055G>C	XP_011517324.1:p.Gly1019Arg
XM_011519023.3:c.3037G>C	XP_011517325.1:p.Gly1013Arg
XM_011519029.3:c.1480G>C	XP_011517331.1:p.Gly494Arg
XM_011519030.3:c.832G>C	XP_011517332.1:p.Gly278Arg
XM_017015134.1:c.3034G>C	XP_016870623.1:p.Gly1012Arg
XM_017015136.2:c.2950G>C	XP_016870625.1:p.Gly984Arg
XM_017015137.1:c.2935G>C	XP_016870626.1:p.Gly979Arg
XM_017015138.1:c.2935G>C	XP_016870627.1:p.Gly979Arg
XM_024447674.1:c.2878G>C	XP_024303442.1:p.Gly960Arg
XM_024447675.1:c.2812G>C	XP_024303443.1:p.Gly938Arg
XM_024447676.1:c.2173G>C	XP_024303444.1:p.Gly725Arg
XM_024447677.1:c.2173G>C	XP_024303445.1:p.Gly725Arg
XM_024447680.1:c.2791G>C	XP_024303448.1:p.Gly931Arg
NM_024757.5:c.3049G>C MANE Select	NP_079033.4:p.Gly1017Arg
NM_001354263.2:c.3028G>C	NP_001341192.1:p.Gly1010Arg