Canonical Allele Identifier: CA375788898

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695384A>G (hg19) ; chr9:g.137800932A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800932A>G , CM000671.2:g.137800932A>G	GRCh38
NC_000009.11:g.140695384A>G , CM000671.1:g.140695384A>G	GRCh37
NC_000009.10:g.139815205A>G	NCBI36
NG_011776.1:g.186941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2660A>G MANE Select	ENSP00000417980.1:p.Asp887Gly
ENST00000636027.1:c.2546A>G	ENSP00000489961.1:p.Asp849Gly
ENST00000637161.1:c.2567A>G	ENSP00000490328.1:p.Asp856Gly
ENST00000637261.1:c.2700A>G	ENSP00000490815.1:n.2700A>G
ENST00000637891.1:c.554A>G	ENSP00000490907.1:p.Asp185Gly
ENST00000637949.1:c.338A>G	ENSP00000489786.1:p.Asp113Gly
ENST00000460843.5:c.2660A>G	ENSP00000417980.1:p.Asp887Gly
ENST00000462942.3:c.1517A>G	ENSP00000436107.1:p.Asp506Gly
ENST00000482340.5:c.230A>G	ENSP00000486748.1:p.Asp77Gly
ENST00000486164.5:c.238A>G
ENST00000488242.2:n.186A>G
ENST00000493484.5:c.230A>G	ENSP00000486503.1:p.Asp77Gly
NM_024757.4:c.2660A>G	NP_079033.4:p.Asp887Gly
XM_005266105.3:c.2651A>G	XP_005266162.1:p.Asp884Gly
XM_005266110.1:c.2567A>G	XP_005266167.1:p.Asp856Gly
XM_006717288.2:c.2642A>G	XP_006717351.1:p.Asp881Gly
XM_011519021.1:c.2669A>G	XP_011517323.1:p.Asp890Gly
XM_011519022.1:c.2666A>G	XP_011517324.1:p.Asp889Gly
XM_011519023.1:c.2648A>G	XP_011517325.1:p.Asp883Gly
XM_011519024.1:c.2591A>G	XP_011517326.1:p.Asp864Gly
XM_011519025.1:c.2567A>G	XP_011517327.1:p.Asp856Gly
XM_011519026.1:c.2525A>G	XP_011517328.1:p.Asp842Gly
XM_011519027.1:c.2669A>G	XP_011517329.1:p.Asp890Gly
XM_011519029.1:c.1091A>G	XP_011517331.1:p.Asp364Gly
XM_011519030.1:c.443A>G	XP_011517332.1:p.Asp148Gly
XM_011519031.1:c.230A>G	XP_011517333.1:p.Asp77Gly
XM_011519032.1:c.230A>G	XP_011517334.1:p.Asp77Gly
XM_011519033.1:c.2504A>G	XP_011517335.1:p.Asp835Gly
NM_001354263.1:c.2639A>G	NP_001341192.1:p.Asp880Gly
XM_005266105.5:c.2651A>G	XP_005266162.1:p.Asp884Gly
XM_011519021.3:c.2669A>G	XP_011517323.1:p.Asp890Gly
XM_011519022.3:c.2666A>G	XP_011517324.1:p.Asp889Gly
XM_011519023.3:c.2648A>G	XP_011517325.1:p.Asp883Gly
XM_011519029.3:c.1091A>G	XP_011517331.1:p.Asp364Gly
XM_011519030.3:c.443A>G	XP_011517332.1:p.Asp148Gly
XM_017015134.1:c.2645A>G	XP_016870623.1:p.Asp882Gly
XM_017015136.2:c.2561A>G	XP_016870625.1:p.Asp854Gly
XM_017015137.1:c.2546A>G	XP_016870626.1:p.Asp849Gly
XM_017015138.1:c.2546A>G	XP_016870627.1:p.Asp849Gly
XM_024447674.1:c.2489A>G	XP_024303442.1:p.Asp830Gly
XM_024447675.1:c.2423A>G	XP_024303443.1:p.Asp808Gly
XM_024447676.1:c.1784A>G	XP_024303444.1:p.Asp595Gly
XM_024447677.1:c.1784A>G	XP_024303445.1:p.Asp595Gly
XM_024447678.1:c.2567A>G	XP_024303446.1:p.Asp856Gly
XM_024447680.1:c.2402A>G	XP_024303448.1:p.Asp801Gly
NM_024757.5:c.2660A>G MANE Select	NP_079033.4:p.Asp887Gly
NM_001354263.2:c.2639A>G	NP_001341192.1:p.Asp880Gly