Canonical Allele Identifier: CA375773441

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140712534G>T (hg19) ; chr9:g.137818082G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137818082G>T , CM000671.2:g.137818082G>T	GRCh38
NC_000009.11:g.140712534G>T , CM000671.1:g.140712534G>T	GRCh37
NC_000009.10:g.139832355G>T	NCBI36
NG_011776.1:g.204091G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.3484G>T MANE Select	ENSP00000417980.1:p.Asp1162Tyr
ENST00000636472.1:n.46G>T
ENST00000637161.1:c.3391G>T	ENSP00000490328.1:p.Asp1131Tyr
ENST00000637261.1:c.4058G>T	ENSP00000490815.1:n.4058G>T
ENST00000637748.1:n.465G>T
ENST00000637891.1:c.1558G>T	ENSP00000490907.1:n.1558G>T
ENST00000460843.5:c.3484G>T	ENSP00000417980.1:p.Asp1162Tyr
ENST00000462942.3:c.2341G>T	ENSP00000436107.1:p.Asp781Tyr
ENST00000475564.5:n.1208G>T
ENST00000494249.5:n.837G>T
NM_024757.4:c.3484G>T	NP_079033.4:p.Asp1162Tyr
XM_005266105.3:c.3475G>T	XP_005266162.1:p.Asp1159Tyr
XM_005266110.1:c.3391G>T	XP_005266167.1:p.Asp1131Tyr
XM_006717288.2:c.3466G>T	XP_006717351.1:p.Asp1156Tyr
XM_011519021.1:c.3493G>T	XP_011517323.1:p.Asp1165Tyr
XM_011519022.1:c.3490G>T	XP_011517324.1:p.Asp1164Tyr
XM_011519023.1:c.3472G>T	XP_011517325.1:p.Asp1158Tyr
XM_011519024.1:c.3415G>T	XP_011517326.1:p.Asp1139Tyr
XM_011519025.1:c.3391G>T	XP_011517327.1:p.Asp1131Tyr
XM_011519026.1:c.3349G>T	XP_011517328.1:p.Asp1117Tyr
XM_011519029.1:c.1915G>T	XP_011517331.1:p.Asp639Tyr
XM_011519030.1:c.1267G>T	XP_011517332.1:p.Asp423Tyr
XM_011519031.1:c.1054G>T	XP_011517333.1:p.Asp352Tyr
XM_011519032.1:c.1054G>T	XP_011517334.1:p.Asp352Tyr
XM_011519033.1:c.3328G>T	XP_011517335.1:p.Asp1110Tyr
XR_930459.1:n.5297-3520C>A
NM_001354263.1:c.3463G>T	NP_001341192.1:p.Asp1155Tyr
XM_005266105.5:c.3475G>T	XP_005266162.1:p.Asp1159Tyr
XM_011519021.3:c.3493G>T	XP_011517323.1:p.Asp1165Tyr
XM_011519022.3:c.3490G>T	XP_011517324.1:p.Asp1164Tyr
XM_011519023.3:c.3472G>T	XP_011517325.1:p.Asp1158Tyr
XM_011519029.3:c.1915G>T	XP_011517331.1:p.Asp639Tyr
XM_011519030.3:c.1267G>T	XP_011517332.1:p.Asp423Tyr
XM_017015134.1:c.3469G>T	XP_016870623.1:p.Asp1157Tyr
XM_017015136.2:c.3385G>T	XP_016870625.1:p.Asp1129Tyr
XM_017015137.1:c.3370G>T	XP_016870626.1:p.Asp1124Tyr
XM_017015138.1:c.3370G>T	XP_016870627.1:p.Asp1124Tyr
XM_024447674.1:c.3313G>T	XP_024303442.1:p.Asp1105Tyr
XM_024447675.1:c.3247G>T	XP_024303443.1:p.Asp1083Tyr
XM_024447676.1:c.2608G>T	XP_024303444.1:p.Asp870Tyr
XM_024447677.1:c.2608G>T	XP_024303445.1:p.Asp870Tyr
XM_024447680.1:c.3226G>T	XP_024303448.1:p.Asp1076Tyr
NM_024757.5:c.3484G>T MANE Select	NP_079033.4:p.Asp1162Tyr
NM_001354263.2:c.3463G>T	NP_001341192.1:p.Asp1155Tyr