Canonical Allele Identifier: CA375769020

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140657184G>T (hg19) ; chr9:g.137762732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137762732G>T , CM000671.2:g.137762732G>T	GRCh38
NC_000009.11:g.140657184G>T , CM000671.1:g.140657184G>T	GRCh37
NC_000009.10:g.139777005G>T	NCBI36
NG_011776.1:g.148741G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1559G>T MANE Select	ENSP00000417980.1:p.Cys520Phe
ENST00000629335.2:c.1559G>T	ENSP00000490056.1:p.Cys520Phe
ENST00000636027.1:c.1445G>T	ENSP00000489961.1:p.Cys482Phe
ENST00000637161.1:c.1466G>T	ENSP00000490328.1:p.Cys489Phe
ENST00000637261.1:c.1599G>T	ENSP00000490815.1:n.1599G>T
ENST00000637977.1:c.1504G>T
ENST00000638071.1:c.1186G>T
ENST00000640639.1:c.728G>T	ENSP00000491823.1:p.Cys243Phe
ENST00000371394.6:c.*1294G>T	ENSP00000485945.1:n.*1294G>T
ENST00000460843.5:c.1559G>T	ENSP00000417980.1:p.Cys520Phe
ENST00000462484.5:c.1559G>T	ENSP00000417328.1:p.Cys520Phe
ENST00000462942.3:c.416G>T	ENSP00000436107.1:p.Cys139Phe
ENST00000465566.2:c.251G>T	ENSP00000486261.1:p.Cys84Phe
ENST00000629808.2:c.652G>T
NM_001145527.1:c.1559G>T	NP_001138999.1:p.Cys520Phe
NM_024757.4:c.1559G>T	NP_079033.4:p.Cys520Phe
XM_005266105.3:c.1550G>T	XP_005266162.1:p.Cys517Phe
XM_005266110.1:c.1466G>T	XP_005266167.1:p.Cys489Phe
XM_006717288.2:c.1541G>T	XP_006717351.1:p.Cys514Phe
XM_011519021.1:c.1568G>T	XP_011517323.1:p.Cys523Phe
XM_011519022.1:c.1565G>T	XP_011517324.1:p.Cys522Phe
XM_011519023.1:c.1547G>T	XP_011517325.1:p.Cys516Phe
XM_011519024.1:c.1490G>T	XP_011517326.1:p.Cys497Phe
XM_011519025.1:c.1466G>T	XP_011517327.1:p.Cys489Phe
XM_011519026.1:c.1568G>T	XP_011517328.1:p.Cys523Phe
XM_011519027.1:c.1568G>T	XP_011517329.1:p.Cys523Phe
XM_011519028.1:c.1568G>T	XP_011517330.1:p.Cys523Phe
XM_011519029.1:c.-11G>T	XP_011517331.1:n.-11G>T
XM_011519033.1:c.1547G>T	XP_011517335.1:p.Cys516Phe
NM_001354259.1:c.1466G>T	NP_001341188.1:p.Cys489Phe
NM_001354263.1:c.1538G>T	NP_001341192.1:p.Cys513Phe
NM_001354611.1:c.1559G>T	NP_001341540.1:p.Cys520Phe
NM_001354612.1:c.1466G>T	NP_001341541.1:p.Cys489Phe
XM_005266105.5:c.1550G>T	XP_005266162.1:p.Cys517Phe
XM_011519021.3:c.1568G>T	XP_011517323.1:p.Cys523Phe
XM_011519022.3:c.1565G>T	XP_011517324.1:p.Cys522Phe
XM_011519023.3:c.1547G>T	XP_011517325.1:p.Cys516Phe
XM_011519029.3:c.-11G>T	XP_011517331.1:n.-11G>T
XM_017015134.1:c.1544G>T	XP_016870623.1:p.Cys515Phe
XM_017015136.2:c.1460G>T	XP_016870625.1:p.Cys487Phe
XM_017015137.1:c.1445G>T	XP_016870626.1:p.Cys482Phe
XM_017015138.1:c.1445G>T	XP_016870627.1:p.Cys482Phe
XM_024447674.1:c.1388G>T	XP_024303442.1:p.Cys463Phe
XM_024447675.1:c.1466G>T	XP_024303443.1:p.Cys489Phe
XM_024447676.1:c.683G>T	XP_024303444.1:p.Cys228Phe
XM_024447677.1:c.683G>T	XP_024303445.1:p.Cys228Phe
XM_024447678.1:c.1466G>T	XP_024303446.1:p.Cys489Phe
XM_024447679.1:c.1466G>T	XP_024303447.1:p.Cys489Phe
XM_024447680.1:c.1445G>T	XP_024303448.1:p.Cys482Phe
NM_024757.5:c.1559G>T MANE Select	NP_079033.4:p.Cys520Phe
NM_001145527.2:c.1559G>T	NP_001138999.1:p.Cys520Phe
NM_001354259.2:c.1466G>T	NP_001341188.1:p.Cys489Phe
NM_001354263.2:c.1538G>T	NP_001341192.1:p.Cys513Phe
NM_001354611.2:c.1559G>T	NP_001341540.1:p.Cys520Phe
NM_001354612.2:c.1466G>T	NP_001341541.1:p.Cys489Phe