Canonical Allele Identifier: CA375773582

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712547A>G (hg19) ; chr9:g.137818095A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818095A>G , CM000671.2:g.137818095A>G	GRCh38
NC_000009.11:g.140712547A>G , CM000671.1:g.140712547A>G	GRCh37
NC_000009.10:g.139832368A>G	NCBI36
NG_011776.1:g.204104A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3497A>G MANE Select	ENSP00000417980.1:p.Asp1166Gly
ENST00000636472.1:n.59A>G
ENST00000637161.1:c.3404A>G	ENSP00000490328.1:p.Asp1135Gly
ENST00000637261.1:c.4071A>G	ENSP00000490815.1:n.4071A>G
ENST00000637748.1:n.478A>G
ENST00000637891.1:c.1571A>G	ENSP00000490907.1:n.1571A>G
ENST00000460843.5:c.3497A>G	ENSP00000417980.1:p.Asp1166Gly
ENST00000462942.3:c.2354A>G	ENSP00000436107.1:p.Asp785Gly
ENST00000475564.5:n.1221A>G
ENST00000494249.5:n.850A>G
NM_024757.4:c.3497A>G	NP_079033.4:p.Asp1166Gly
XM_005266105.3:c.3488A>G	XP_005266162.1:p.Asp1163Gly
XM_005266110.1:c.3404A>G	XP_005266167.1:p.Asp1135Gly
XM_006717288.2:c.3479A>G	XP_006717351.1:p.Asp1160Gly
XM_011519021.1:c.3506A>G	XP_011517323.1:p.Asp1169Gly
XM_011519022.1:c.3503A>G	XP_011517324.1:p.Asp1168Gly
XM_011519023.1:c.3485A>G	XP_011517325.1:p.Asp1162Gly
XM_011519024.1:c.3428A>G	XP_011517326.1:p.Asp1143Gly
XM_011519025.1:c.3404A>G	XP_011517327.1:p.Asp1135Gly
XM_011519026.1:c.3362A>G	XP_011517328.1:p.Asp1121Gly
XM_011519029.1:c.1928A>G	XP_011517331.1:p.Asp643Gly
XM_011519030.1:c.1280A>G	XP_011517332.1:p.Asp427Gly
XM_011519031.1:c.1067A>G	XP_011517333.1:p.Asp356Gly
XM_011519032.1:c.1067A>G	XP_011517334.1:p.Asp356Gly
XM_011519033.1:c.3341A>G	XP_011517335.1:p.Asp1114Gly
XR_930459.1:n.5297-3533T>C
NM_001354263.1:c.3476A>G	NP_001341192.1:p.Asp1159Gly
XM_005266105.5:c.3488A>G	XP_005266162.1:p.Asp1163Gly
XM_011519021.3:c.3506A>G	XP_011517323.1:p.Asp1169Gly
XM_011519022.3:c.3503A>G	XP_011517324.1:p.Asp1168Gly
XM_011519023.3:c.3485A>G	XP_011517325.1:p.Asp1162Gly
XM_011519029.3:c.1928A>G	XP_011517331.1:p.Asp643Gly
XM_011519030.3:c.1280A>G	XP_011517332.1:p.Asp427Gly
XM_017015134.1:c.3482A>G	XP_016870623.1:p.Asp1161Gly
XM_017015136.2:c.3398A>G	XP_016870625.1:p.Asp1133Gly
XM_017015137.1:c.3383A>G	XP_016870626.1:p.Asp1128Gly
XM_017015138.1:c.3383A>G	XP_016870627.1:p.Asp1128Gly
XM_024447674.1:c.3326A>G	XP_024303442.1:p.Asp1109Gly
XM_024447675.1:c.3260A>G	XP_024303443.1:p.Asp1087Gly
XM_024447676.1:c.2621A>G	XP_024303444.1:p.Asp874Gly
XM_024447677.1:c.2621A>G	XP_024303445.1:p.Asp874Gly
XM_024447680.1:c.3239A>G	XP_024303448.1:p.Asp1080Gly
NM_024757.5:c.3497A>G MANE Select	NP_079033.4:p.Asp1166Gly
NM_001354263.2:c.3476A>G	NP_001341192.1:p.Asp1159Gly