Canonical Allele Identifier: CA375788717

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695338G>T (hg19) ; chr9:g.137800886G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800886G>T , CM000671.2:g.137800886G>T	GRCh38
NC_000009.11:g.140695338G>T , CM000671.1:g.140695338G>T	GRCh37
NC_000009.10:g.139815159G>T	NCBI36
NG_011776.1:g.186895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2614G>T MANE Select	ENSP00000417980.1:p.Gly872Ter
ENST00000636027.1:c.2500G>T	ENSP00000489961.1:p.Gly834Ter
ENST00000637161.1:c.2521G>T	ENSP00000490328.1:p.Gly841Ter
ENST00000637261.1:c.2654G>T	ENSP00000490815.1:n.2654G>T
ENST00000637891.1:c.508G>T	ENSP00000490907.1:p.Gly170Ter
ENST00000637949.1:c.292G>T	ENSP00000489786.1:p.Gly98Ter
ENST00000460843.5:c.2614G>T	ENSP00000417980.1:p.Gly872Ter
ENST00000462942.3:c.1471G>T	ENSP00000436107.1:p.Gly491Ter
ENST00000482340.5:c.184G>T	ENSP00000486748.1:p.Gly62Ter
ENST00000486164.5:c.192G>T
ENST00000488242.2:n.140G>T
ENST00000493484.5:c.184G>T	ENSP00000486503.1:p.Gly62Ter
NM_024757.4:c.2614G>T	NP_079033.4:p.Gly872Ter
XM_005266105.3:c.2605G>T	XP_005266162.1:p.Gly869Ter
XM_005266110.1:c.2521G>T	XP_005266167.1:p.Gly841Ter
XM_006717288.2:c.2596G>T	XP_006717351.1:p.Gly866Ter
XM_011519021.1:c.2623G>T	XP_011517323.1:p.Gly875Ter
XM_011519022.1:c.2620G>T	XP_011517324.1:p.Gly874Ter
XM_011519023.1:c.2602G>T	XP_011517325.1:p.Gly868Ter
XM_011519024.1:c.2545G>T	XP_011517326.1:p.Gly849Ter
XM_011519025.1:c.2521G>T	XP_011517327.1:p.Gly841Ter
XM_011519026.1:c.2479G>T	XP_011517328.1:p.Gly827Ter
XM_011519027.1:c.2623G>T	XP_011517329.1:p.Gly875Ter
XM_011519029.1:c.1045G>T	XP_011517331.1:p.Gly349Ter
XM_011519030.1:c.397G>T	XP_011517332.1:p.Gly133Ter
XM_011519031.1:c.184G>T	XP_011517333.1:p.Gly62Ter
XM_011519032.1:c.184G>T	XP_011517334.1:p.Gly62Ter
XM_011519033.1:c.2458G>T	XP_011517335.1:p.Gly820Ter
NM_001354263.1:c.2593G>T	NP_001341192.1:p.Gly865Ter
XM_005266105.5:c.2605G>T	XP_005266162.1:p.Gly869Ter
XM_011519021.3:c.2623G>T	XP_011517323.1:p.Gly875Ter
XM_011519022.3:c.2620G>T	XP_011517324.1:p.Gly874Ter
XM_011519023.3:c.2602G>T	XP_011517325.1:p.Gly868Ter
XM_011519029.3:c.1045G>T	XP_011517331.1:p.Gly349Ter
XM_011519030.3:c.397G>T	XP_011517332.1:p.Gly133Ter
XM_017015134.1:c.2599G>T	XP_016870623.1:p.Gly867Ter
XM_017015136.2:c.2515G>T	XP_016870625.1:p.Gly839Ter
XM_017015137.1:c.2500G>T	XP_016870626.1:p.Gly834Ter
XM_017015138.1:c.2500G>T	XP_016870627.1:p.Gly834Ter
XM_024447674.1:c.2443G>T	XP_024303442.1:p.Gly815Ter
XM_024447675.1:c.2377G>T	XP_024303443.1:p.Gly793Ter
XM_024447676.1:c.1738G>T	XP_024303444.1:p.Gly580Ter
XM_024447677.1:c.1738G>T	XP_024303445.1:p.Gly580Ter
XM_024447678.1:c.2521G>T	XP_024303446.1:p.Gly841Ter
XM_024447680.1:c.2356G>T	XP_024303448.1:p.Gly786Ter
NM_024757.5:c.2614G>T MANE Select	NP_079033.4:p.Gly872Ter
NM_001354263.2:c.2593G>T	NP_001341192.1:p.Gly865Ter