Canonical Allele Identifier: CA375793228

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707477T>A (hg19) ; chr9:g.137813025T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813025T>A , CM000671.2:g.137813025T>A	GRCh38
NC_000009.11:g.140707477T>A , CM000671.1:g.140707477T>A	GRCh37
NC_000009.10:g.139827298T>A	NCBI36
NG_011776.1:g.199034T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2887T>A MANE Select	ENSP00000417980.1:p.Ser963Thr
ENST00000636027.1:c.2773T>A	ENSP00000489961.1:p.Ser925Thr
ENST00000637161.1:c.2794T>A	ENSP00000490328.1:p.Ser932Thr
ENST00000637261.1:c.2927T>A	ENSP00000490815.1:n.2927T>A
ENST00000637891.1:c.781T>A	ENSP00000490907.1:p.Ser261Thr
ENST00000460843.5:c.2887T>A	ENSP00000417980.1:p.Ser963Thr
ENST00000462942.3:c.1744T>A	ENSP00000436107.1:p.Ser582Thr
ENST00000486164.5:c.574T>A
ENST00000488242.2:n.413T>A
NM_024757.4:c.2887T>A	NP_079033.4:p.Ser963Thr
XM_005266105.3:c.2878T>A	XP_005266162.1:p.Ser960Thr
XM_005266110.1:c.2794T>A	XP_005266167.1:p.Ser932Thr
XM_006717288.2:c.2869T>A	XP_006717351.1:p.Ser957Thr
XM_011519021.1:c.2896T>A	XP_011517323.1:p.Ser966Thr
XM_011519022.1:c.2893T>A	XP_011517324.1:p.Ser965Thr
XM_011519023.1:c.2875T>A	XP_011517325.1:p.Ser959Thr
XM_011519024.1:c.2818T>A	XP_011517326.1:p.Ser940Thr
XM_011519025.1:c.2794T>A	XP_011517327.1:p.Ser932Thr
XM_011519026.1:c.2752T>A	XP_011517328.1:p.Ser918Thr
XM_011519029.1:c.1318T>A	XP_011517331.1:p.Ser440Thr
XM_011519030.1:c.670T>A	XP_011517332.1:p.Ser224Thr
XM_011519031.1:c.457T>A	XP_011517333.1:p.Ser153Thr
XM_011519032.1:c.457T>A	XP_011517334.1:p.Ser153Thr
XM_011519033.1:c.2731T>A	XP_011517335.1:p.Ser911Thr
NM_001354263.1:c.2866T>A	NP_001341192.1:p.Ser956Thr
XM_005266105.5:c.2878T>A	XP_005266162.1:p.Ser960Thr
XM_011519021.3:c.2896T>A	XP_011517323.1:p.Ser966Thr
XM_011519022.3:c.2893T>A	XP_011517324.1:p.Ser965Thr
XM_011519023.3:c.2875T>A	XP_011517325.1:p.Ser959Thr
XM_011519029.3:c.1318T>A	XP_011517331.1:p.Ser440Thr
XM_011519030.3:c.670T>A	XP_011517332.1:p.Ser224Thr
XM_017015134.1:c.2872T>A	XP_016870623.1:p.Ser958Thr
XM_017015136.2:c.2788T>A	XP_016870625.1:p.Ser930Thr
XM_017015137.1:c.2773T>A	XP_016870626.1:p.Ser925Thr
XM_017015138.1:c.2773T>A	XP_016870627.1:p.Ser925Thr
XM_024447674.1:c.2716T>A	XP_024303442.1:p.Ser906Thr
XM_024447675.1:c.2650T>A	XP_024303443.1:p.Ser884Thr
XM_024447676.1:c.2011T>A	XP_024303444.1:p.Ser671Thr
XM_024447677.1:c.2011T>A	XP_024303445.1:p.Ser671Thr
XM_024447680.1:c.2629T>A	XP_024303448.1:p.Ser877Thr
NM_024757.5:c.2887T>A MANE Select	NP_079033.4:p.Ser963Thr
NM_001354263.2:c.2866T>A	NP_001341192.1:p.Ser956Thr