Canonical Allele Identifier: CA375793971

Gene: EHMT1

Linked Data

• dbSNP Id: rs1954655891
• MyVariant Identifiers: chr9:g.140707879T>G (hg19) ; chr9:g.137813427T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813427T>G , CM000671.2:g.137813427T>G	GRCh38
NC_000009.11:g.140707879T>G , CM000671.1:g.140707879T>G	GRCh37
NC_000009.10:g.139827700T>G	NCBI36
NG_011776.1:g.199436T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.3077T>G MANE Select	ENSP00000417980.1:p.Val1026Gly
ENST00000637161.1:c.2984T>G	ENSP00000490328.1:p.Val995Gly
ENST00000637261.1:c.3117T>G	ENSP00000490815.1:n.3117T>G
ENST00000637891.1:c.971T>G	ENSP00000490907.1:p.Val324Gly
ENST00000460843.5:c.3077T>G	ENSP00000417980.1:p.Val1026Gly
ENST00000462942.3:c.1934T>G	ENSP00000436107.1:p.Val645Gly
ENST00000486164.5:c.764T>G
ENST00000488242.2:n.603T>G
NM_024757.4:c.3077T>G	NP_079033.4:p.Val1026Gly
XM_005266105.3:c.3068T>G	XP_005266162.1:p.Val1023Gly
XM_005266110.1:c.2984T>G	XP_005266167.1:p.Val995Gly
XM_006717288.2:c.3059T>G	XP_006717351.1:p.Val1020Gly
XM_011519021.1:c.3086T>G	XP_011517323.1:p.Val1029Gly
XM_011519022.1:c.3083T>G	XP_011517324.1:p.Val1028Gly
XM_011519023.1:c.3065T>G	XP_011517325.1:p.Val1022Gly
XM_011519024.1:c.3008T>G	XP_011517326.1:p.Val1003Gly
XM_011519025.1:c.2984T>G	XP_011517327.1:p.Val995Gly
XM_011519026.1:c.2942T>G	XP_011517328.1:p.Val981Gly
XM_011519029.1:c.1508T>G	XP_011517331.1:p.Val503Gly
XM_011519030.1:c.860T>G	XP_011517332.1:p.Val287Gly
XM_011519031.1:c.647T>G	XP_011517333.1:p.Val216Gly
XM_011519032.1:c.647T>G	XP_011517334.1:p.Val216Gly
XM_011519033.1:c.2921T>G	XP_011517335.1:p.Val974Gly
NM_001354263.1:c.3056T>G	NP_001341192.1:p.Val1019Gly
XM_005266105.5:c.3068T>G	XP_005266162.1:p.Val1023Gly
XM_011519021.3:c.3086T>G	XP_011517323.1:p.Val1029Gly
XM_011519022.3:c.3083T>G	XP_011517324.1:p.Val1028Gly
XM_011519023.3:c.3065T>G	XP_011517325.1:p.Val1022Gly
XM_011519029.3:c.1508T>G	XP_011517331.1:p.Val503Gly
XM_011519030.3:c.860T>G	XP_011517332.1:p.Val287Gly
XM_017015134.1:c.3062T>G	XP_016870623.1:p.Val1021Gly
XM_017015136.2:c.2978T>G	XP_016870625.1:p.Val993Gly
XM_017015137.1:c.2963T>G	XP_016870626.1:p.Val988Gly
XM_017015138.1:c.2963T>G	XP_016870627.1:p.Val988Gly
XM_024447674.1:c.2906T>G	XP_024303442.1:p.Val969Gly
XM_024447675.1:c.2840T>G	XP_024303443.1:p.Val947Gly
XM_024447676.1:c.2201T>G	XP_024303444.1:p.Val734Gly
XM_024447677.1:c.2201T>G	XP_024303445.1:p.Val734Gly
XM_024447680.1:c.2819T>G	XP_024303448.1:p.Val940Gly
NM_024757.5:c.3077T>G MANE Select	NP_079033.4:p.Val1026Gly
NM_001354263.2:c.3056T>G	NP_001341192.1:p.Val1019Gly