Canonical Allele Identifier: CA375773744

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712567T>G (hg19) ; chr9:g.137818115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818115T>G , CM000671.2:g.137818115T>G	GRCh38
NC_000009.11:g.140712567T>G , CM000671.1:g.140712567T>G	GRCh37
NC_000009.10:g.139832388T>G	NCBI36
NG_011776.1:g.204124T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3517T>G MANE Select	ENSP00000417980.1:p.Tyr1173Asp
ENST00000636472.1:n.79T>G
ENST00000636526.1:n.3T>G
ENST00000637161.1:c.3424T>G	ENSP00000490328.1:p.Tyr1142Asp
ENST00000637261.1:c.4091T>G	ENSP00000490815.1:n.4091T>G
ENST00000637748.1:n.498T>G
ENST00000637891.1:c.1591T>G	ENSP00000490907.1:n.1591T>G
ENST00000460843.5:c.3517T>G	ENSP00000417980.1:p.Tyr1173Asp
ENST00000462942.3:c.2374T>G	ENSP00000436107.1:p.Tyr792Asp
ENST00000475564.5:n.1241T>G
ENST00000494249.5:n.870T>G
NM_024757.4:c.3517T>G	NP_079033.4:p.Tyr1173Asp
XM_005266105.3:c.3508T>G	XP_005266162.1:p.Tyr1170Asp
XM_005266110.1:c.3424T>G	XP_005266167.1:p.Tyr1142Asp
XM_006717288.2:c.3499T>G	XP_006717351.1:p.Tyr1167Asp
XM_011519021.1:c.3526T>G	XP_011517323.1:p.Tyr1176Asp
XM_011519022.1:c.3523T>G	XP_011517324.1:p.Tyr1175Asp
XM_011519023.1:c.3505T>G	XP_011517325.1:p.Tyr1169Asp
XM_011519024.1:c.3448T>G	XP_011517326.1:p.Tyr1150Asp
XM_011519025.1:c.3424T>G	XP_011517327.1:p.Tyr1142Asp
XM_011519026.1:c.3382T>G	XP_011517328.1:p.Tyr1128Asp
XM_011519029.1:c.1948T>G	XP_011517331.1:p.Tyr650Asp
XM_011519030.1:c.1300T>G	XP_011517332.1:p.Tyr434Asp
XM_011519031.1:c.1087T>G	XP_011517333.1:p.Tyr363Asp
XM_011519032.1:c.1087T>G	XP_011517334.1:p.Tyr363Asp
XM_011519033.1:c.3361T>G	XP_011517335.1:p.Tyr1121Asp
XR_930459.1:n.5297-3553A>C
NM_001354263.1:c.3496T>G	NP_001341192.1:p.Tyr1166Asp
XM_005266105.5:c.3508T>G	XP_005266162.1:p.Tyr1170Asp
XM_011519021.3:c.3526T>G	XP_011517323.1:p.Tyr1176Asp
XM_011519022.3:c.3523T>G	XP_011517324.1:p.Tyr1175Asp
XM_011519023.3:c.3505T>G	XP_011517325.1:p.Tyr1169Asp
XM_011519029.3:c.1948T>G	XP_011517331.1:p.Tyr650Asp
XM_011519030.3:c.1300T>G	XP_011517332.1:p.Tyr434Asp
XM_017015134.1:c.3502T>G	XP_016870623.1:p.Tyr1168Asp
XM_017015136.2:c.3418T>G	XP_016870625.1:p.Tyr1140Asp
XM_017015137.1:c.3403T>G	XP_016870626.1:p.Tyr1135Asp
XM_017015138.1:c.3403T>G	XP_016870627.1:p.Tyr1135Asp
XM_024447674.1:c.3346T>G	XP_024303442.1:p.Tyr1116Asp
XM_024447675.1:c.3280T>G	XP_024303443.1:p.Tyr1094Asp
XM_024447676.1:c.2641T>G	XP_024303444.1:p.Tyr881Asp
XM_024447677.1:c.2641T>G	XP_024303445.1:p.Tyr881Asp
XM_024447680.1:c.3259T>G	XP_024303448.1:p.Tyr1087Asp
NM_024757.5:c.3517T>G MANE Select	NP_079033.4:p.Tyr1173Asp
NM_001354263.2:c.3496T>G	NP_001341192.1:p.Tyr1166Asp