Canonical Allele Identifier: CA375793197

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707468T>A (hg19) ; chr9:g.137813016T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813016T>A , CM000671.2:g.137813016T>A	GRCh38
NC_000009.11:g.140707468T>A , CM000671.1:g.140707468T>A	GRCh37
NC_000009.10:g.139827289T>A	NCBI36
NG_011776.1:g.199025T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2878T>A MANE Select	ENSP00000417980.1:p.Ser960Thr
ENST00000636027.1:c.2764T>A	ENSP00000489961.1:p.Ser922Thr
ENST00000637161.1:c.2785T>A	ENSP00000490328.1:p.Ser929Thr
ENST00000637261.1:c.2918T>A	ENSP00000490815.1:n.2918T>A
ENST00000637891.1:c.772T>A	ENSP00000490907.1:p.Ser258Thr
ENST00000460843.5:c.2878T>A	ENSP00000417980.1:p.Ser960Thr
ENST00000462942.3:c.1735T>A	ENSP00000436107.1:p.Ser579Thr
ENST00000486164.5:c.565T>A
ENST00000488242.2:n.404T>A
NM_024757.4:c.2878T>A	NP_079033.4:p.Ser960Thr
XM_005266105.3:c.2869T>A	XP_005266162.1:p.Ser957Thr
XM_005266110.1:c.2785T>A	XP_005266167.1:p.Ser929Thr
XM_006717288.2:c.2860T>A	XP_006717351.1:p.Ser954Thr
XM_011519021.1:c.2887T>A	XP_011517323.1:p.Ser963Thr
XM_011519022.1:c.2884T>A	XP_011517324.1:p.Ser962Thr
XM_011519023.1:c.2866T>A	XP_011517325.1:p.Ser956Thr
XM_011519024.1:c.2809T>A	XP_011517326.1:p.Ser937Thr
XM_011519025.1:c.2785T>A	XP_011517327.1:p.Ser929Thr
XM_011519026.1:c.2743T>A	XP_011517328.1:p.Ser915Thr
XM_011519029.1:c.1309T>A	XP_011517331.1:p.Ser437Thr
XM_011519030.1:c.661T>A	XP_011517332.1:p.Ser221Thr
XM_011519031.1:c.448T>A	XP_011517333.1:p.Ser150Thr
XM_011519032.1:c.448T>A	XP_011517334.1:p.Ser150Thr
XM_011519033.1:c.2722T>A	XP_011517335.1:p.Ser908Thr
NM_001354263.1:c.2857T>A	NP_001341192.1:p.Ser953Thr
XM_005266105.5:c.2869T>A	XP_005266162.1:p.Ser957Thr
XM_011519021.3:c.2887T>A	XP_011517323.1:p.Ser963Thr
XM_011519022.3:c.2884T>A	XP_011517324.1:p.Ser962Thr
XM_011519023.3:c.2866T>A	XP_011517325.1:p.Ser956Thr
XM_011519029.3:c.1309T>A	XP_011517331.1:p.Ser437Thr
XM_011519030.3:c.661T>A	XP_011517332.1:p.Ser221Thr
XM_017015134.1:c.2863T>A	XP_016870623.1:p.Ser955Thr
XM_017015136.2:c.2779T>A	XP_016870625.1:p.Ser927Thr
XM_017015137.1:c.2764T>A	XP_016870626.1:p.Ser922Thr
XM_017015138.1:c.2764T>A	XP_016870627.1:p.Ser922Thr
XM_024447674.1:c.2707T>A	XP_024303442.1:p.Ser903Thr
XM_024447675.1:c.2641T>A	XP_024303443.1:p.Ser881Thr
XM_024447676.1:c.2002T>A	XP_024303444.1:p.Ser668Thr
XM_024447677.1:c.2002T>A	XP_024303445.1:p.Ser668Thr
XM_024447680.1:c.2620T>A	XP_024303448.1:p.Ser874Thr
NM_024757.5:c.2878T>A MANE Select	NP_079033.4:p.Ser960Thr
NM_001354263.2:c.2857T>A	NP_001341192.1:p.Ser953Thr