Canonical Allele Identifier: CA375794414

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707939T>G (hg19) ; chr9:g.137813487T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813487T>G , CM000671.2:g.137813487T>G	GRCh38
NC_000009.11:g.140707939T>G , CM000671.1:g.140707939T>G	GRCh37
NC_000009.10:g.139827760T>G	NCBI36
NG_011776.1:g.199496T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3137T>G MANE Select	ENSP00000417980.1:p.Val1046Gly
ENST00000637161.1:c.3044T>G	ENSP00000490328.1:p.Val1015Gly
ENST00000637261.1:c.3177T>G	ENSP00000490815.1:n.3177T>G
ENST00000637891.1:c.1031T>G	ENSP00000490907.1:p.Val344Gly
ENST00000460843.5:c.3137T>G	ENSP00000417980.1:p.Val1046Gly
ENST00000462942.3:c.1994T>G	ENSP00000436107.1:p.Val665Gly
ENST00000488242.2:n.663T>G
NM_024757.4:c.3137T>G	NP_079033.4:p.Val1046Gly
XM_005266105.3:c.3128T>G	XP_005266162.1:p.Val1043Gly
XM_005266110.1:c.3044T>G	XP_005266167.1:p.Val1015Gly
XM_006717288.2:c.3119T>G	XP_006717351.1:p.Val1040Gly
XM_011519021.1:c.3146T>G	XP_011517323.1:p.Val1049Gly
XM_011519022.1:c.3143T>G	XP_011517324.1:p.Val1048Gly
XM_011519023.1:c.3125T>G	XP_011517325.1:p.Val1042Gly
XM_011519024.1:c.3068T>G	XP_011517326.1:p.Val1023Gly
XM_011519025.1:c.3044T>G	XP_011517327.1:p.Val1015Gly
XM_011519026.1:c.3002T>G	XP_011517328.1:p.Val1001Gly
XM_011519029.1:c.1568T>G	XP_011517331.1:p.Val523Gly
XM_011519030.1:c.920T>G	XP_011517332.1:p.Val307Gly
XM_011519031.1:c.707T>G	XP_011517333.1:p.Val236Gly
XM_011519032.1:c.707T>G	XP_011517334.1:p.Val236Gly
XM_011519033.1:c.2981T>G	XP_011517335.1:p.Val994Gly
NM_001354263.1:c.3116T>G	NP_001341192.1:p.Val1039Gly
XM_005266105.5:c.3128T>G	XP_005266162.1:p.Val1043Gly
XM_011519021.3:c.3146T>G	XP_011517323.1:p.Val1049Gly
XM_011519022.3:c.3143T>G	XP_011517324.1:p.Val1048Gly
XM_011519023.3:c.3125T>G	XP_011517325.1:p.Val1042Gly
XM_011519029.3:c.1568T>G	XP_011517331.1:p.Val523Gly
XM_011519030.3:c.920T>G	XP_011517332.1:p.Val307Gly
XM_017015134.1:c.3122T>G	XP_016870623.1:p.Val1041Gly
XM_017015136.2:c.3038T>G	XP_016870625.1:p.Val1013Gly
XM_017015137.1:c.3023T>G	XP_016870626.1:p.Val1008Gly
XM_017015138.1:c.3023T>G	XP_016870627.1:p.Val1008Gly
XM_024447674.1:c.2966T>G	XP_024303442.1:p.Val989Gly
XM_024447675.1:c.2900T>G	XP_024303443.1:p.Val967Gly
XM_024447676.1:c.2261T>G	XP_024303444.1:p.Val754Gly
XM_024447677.1:c.2261T>G	XP_024303445.1:p.Val754Gly
XM_024447680.1:c.2879T>G	XP_024303448.1:p.Val960Gly
NM_024757.5:c.3137T>G MANE Select	NP_079033.4:p.Val1046Gly
NM_001354263.2:c.3116T>G	NP_001341192.1:p.Val1039Gly