Canonical Allele Identifier: CA375794325

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707926T>A (hg19) ; chr9:g.137813474T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813474T>A , CM000671.2:g.137813474T>A	GRCh38
NC_000009.11:g.140707926T>A , CM000671.1:g.140707926T>A	GRCh37
NC_000009.10:g.139827747T>A	NCBI36
NG_011776.1:g.199483T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3124T>A MANE Select	ENSP00000417980.1:p.Ser1042Thr
ENST00000637161.1:c.3031T>A	ENSP00000490328.1:p.Ser1011Thr
ENST00000637261.1:c.3164T>A	ENSP00000490815.1:n.3164T>A
ENST00000637891.1:c.1018T>A	ENSP00000490907.1:p.Ser340Thr
ENST00000460843.5:c.3124T>A	ENSP00000417980.1:p.Ser1042Thr
ENST00000462942.3:c.1981T>A	ENSP00000436107.1:p.Ser661Thr
ENST00000488242.2:n.650T>A
NM_024757.4:c.3124T>A	NP_079033.4:p.Ser1042Thr
XM_005266105.3:c.3115T>A	XP_005266162.1:p.Ser1039Thr
XM_005266110.1:c.3031T>A	XP_005266167.1:p.Ser1011Thr
XM_006717288.2:c.3106T>A	XP_006717351.1:p.Ser1036Thr
XM_011519021.1:c.3133T>A	XP_011517323.1:p.Ser1045Thr
XM_011519022.1:c.3130T>A	XP_011517324.1:p.Ser1044Thr
XM_011519023.1:c.3112T>A	XP_011517325.1:p.Ser1038Thr
XM_011519024.1:c.3055T>A	XP_011517326.1:p.Ser1019Thr
XM_011519025.1:c.3031T>A	XP_011517327.1:p.Ser1011Thr
XM_011519026.1:c.2989T>A	XP_011517328.1:p.Ser997Thr
XM_011519029.1:c.1555T>A	XP_011517331.1:p.Ser519Thr
XM_011519030.1:c.907T>A	XP_011517332.1:p.Ser303Thr
XM_011519031.1:c.694T>A	XP_011517333.1:p.Ser232Thr
XM_011519032.1:c.694T>A	XP_011517334.1:p.Ser232Thr
XM_011519033.1:c.2968T>A	XP_011517335.1:p.Ser990Thr
NM_001354263.1:c.3103T>A	NP_001341192.1:p.Ser1035Thr
XM_005266105.5:c.3115T>A	XP_005266162.1:p.Ser1039Thr
XM_011519021.3:c.3133T>A	XP_011517323.1:p.Ser1045Thr
XM_011519022.3:c.3130T>A	XP_011517324.1:p.Ser1044Thr
XM_011519023.3:c.3112T>A	XP_011517325.1:p.Ser1038Thr
XM_011519029.3:c.1555T>A	XP_011517331.1:p.Ser519Thr
XM_011519030.3:c.907T>A	XP_011517332.1:p.Ser303Thr
XM_017015134.1:c.3109T>A	XP_016870623.1:p.Ser1037Thr
XM_017015136.2:c.3025T>A	XP_016870625.1:p.Ser1009Thr
XM_017015137.1:c.3010T>A	XP_016870626.1:p.Ser1004Thr
XM_017015138.1:c.3010T>A	XP_016870627.1:p.Ser1004Thr
XM_024447674.1:c.2953T>A	XP_024303442.1:p.Ser985Thr
XM_024447675.1:c.2887T>A	XP_024303443.1:p.Ser963Thr
XM_024447676.1:c.2248T>A	XP_024303444.1:p.Ser750Thr
XM_024447677.1:c.2248T>A	XP_024303445.1:p.Ser750Thr
XM_024447680.1:c.2866T>A	XP_024303448.1:p.Ser956Thr
NM_024757.5:c.3124T>A MANE Select	NP_079033.4:p.Ser1042Thr
NM_001354263.2:c.3103T>A	NP_001341192.1:p.Ser1035Thr