Canonical Allele Identifier: CA375788796

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695360G>C (hg19) ; chr9:g.137800908G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800908G>C , CM000671.2:g.137800908G>C	GRCh38
NC_000009.11:g.140695360G>C , CM000671.1:g.140695360G>C	GRCh37
NC_000009.10:g.139815181G>C	NCBI36
NG_011776.1:g.186917G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2636G>C MANE Select	ENSP00000417980.1:p.Trp879Ser
ENST00000636027.1:c.2522G>C	ENSP00000489961.1:p.Trp841Ser
ENST00000637161.1:c.2543G>C	ENSP00000490328.1:p.Trp848Ser
ENST00000637261.1:c.2676G>C	ENSP00000490815.1:n.2676G>C
ENST00000637891.1:c.530G>C	ENSP00000490907.1:p.Trp177Ser
ENST00000637949.1:c.314G>C	ENSP00000489786.1:p.Trp105Ser
ENST00000460843.5:c.2636G>C	ENSP00000417980.1:p.Trp879Ser
ENST00000462942.3:c.1493G>C	ENSP00000436107.1:p.Trp498Ser
ENST00000482340.5:c.206G>C	ENSP00000486748.1:p.Trp69Ser
ENST00000486164.5:c.214G>C
ENST00000488242.2:n.162G>C
ENST00000493484.5:c.206G>C	ENSP00000486503.1:p.Trp69Ser
NM_024757.4:c.2636G>C	NP_079033.4:p.Trp879Ser
XM_005266105.3:c.2627G>C	XP_005266162.1:p.Trp876Ser
XM_005266110.1:c.2543G>C	XP_005266167.1:p.Trp848Ser
XM_006717288.2:c.2618G>C	XP_006717351.1:p.Trp873Ser
XM_011519021.1:c.2645G>C	XP_011517323.1:p.Trp882Ser
XM_011519022.1:c.2642G>C	XP_011517324.1:p.Trp881Ser
XM_011519023.1:c.2624G>C	XP_011517325.1:p.Trp875Ser
XM_011519024.1:c.2567G>C	XP_011517326.1:p.Trp856Ser
XM_011519025.1:c.2543G>C	XP_011517327.1:p.Trp848Ser
XM_011519026.1:c.2501G>C	XP_011517328.1:p.Trp834Ser
XM_011519027.1:c.2645G>C	XP_011517329.1:p.Trp882Ser
XM_011519029.1:c.1067G>C	XP_011517331.1:p.Trp356Ser
XM_011519030.1:c.419G>C	XP_011517332.1:p.Trp140Ser
XM_011519031.1:c.206G>C	XP_011517333.1:p.Trp69Ser
XM_011519032.1:c.206G>C	XP_011517334.1:p.Trp69Ser
XM_011519033.1:c.2480G>C	XP_011517335.1:p.Trp827Ser
NM_001354263.1:c.2615G>C	NP_001341192.1:p.Trp872Ser
XM_005266105.5:c.2627G>C	XP_005266162.1:p.Trp876Ser
XM_011519021.3:c.2645G>C	XP_011517323.1:p.Trp882Ser
XM_011519022.3:c.2642G>C	XP_011517324.1:p.Trp881Ser
XM_011519023.3:c.2624G>C	XP_011517325.1:p.Trp875Ser
XM_011519029.3:c.1067G>C	XP_011517331.1:p.Trp356Ser
XM_011519030.3:c.419G>C	XP_011517332.1:p.Trp140Ser
XM_017015134.1:c.2621G>C	XP_016870623.1:p.Trp874Ser
XM_017015136.2:c.2537G>C	XP_016870625.1:p.Trp846Ser
XM_017015137.1:c.2522G>C	XP_016870626.1:p.Trp841Ser
XM_017015138.1:c.2522G>C	XP_016870627.1:p.Trp841Ser
XM_024447674.1:c.2465G>C	XP_024303442.1:p.Trp822Ser
XM_024447675.1:c.2399G>C	XP_024303443.1:p.Trp800Ser
XM_024447676.1:c.1760G>C	XP_024303444.1:p.Trp587Ser
XM_024447677.1:c.1760G>C	XP_024303445.1:p.Trp587Ser
XM_024447678.1:c.2543G>C	XP_024303446.1:p.Trp848Ser
XM_024447680.1:c.2378G>C	XP_024303448.1:p.Trp793Ser
NM_024757.5:c.2636G>C MANE Select	NP_079033.4:p.Trp879Ser
NM_001354263.2:c.2615G>C	NP_001341192.1:p.Trp872Ser