Canonical Allele Identifier: CA375776232

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671163C>T (hg19) ; chr9:g.137776711C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776711C>T , CM000671.2:g.137776711C>T	GRCh38
NC_000009.11:g.140671163C>T , CM000671.1:g.140671163C>T	GRCh37
NC_000009.10:g.139790984C>T	NCBI36
NG_011776.1:g.162720C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1885C>T MANE Select	ENSP00000417980.1:p.His629Tyr
ENST00000636027.1:c.1771C>T	ENSP00000489961.1:p.His591Tyr
ENST00000637161.1:c.1792C>T	ENSP00000490328.1:p.His598Tyr
ENST00000637261.1:c.1925C>T	ENSP00000490815.1:n.1925C>T
ENST00000638071.1:c.1512C>T
ENST00000640639.1:c.1054C>T	ENSP00000491823.1:p.His352Tyr
ENST00000371394.6:c.*1620C>T	ENSP00000485945.1:n.*1620C>T
ENST00000460843.5:c.1885C>T	ENSP00000417980.1:p.His629Tyr
ENST00000462484.5:c.1885C>T	ENSP00000417328.1:p.His629Tyr
ENST00000462942.3:c.742C>T	ENSP00000436107.1:p.His248Tyr
ENST00000465566.2:c.433C>T	ENSP00000486261.1:p.His145Tyr
ENST00000626603.1:n.1738G>A
NM_001145527.1:c.1885C>T	NP_001138999.1:p.His629Tyr
NM_024757.4:c.1885C>T	NP_079033.4:p.His629Tyr
XM_005266105.3:c.1876C>T	XP_005266162.1:p.His626Tyr
XM_005266110.1:c.1792C>T	XP_005266167.1:p.His598Tyr
XM_006717288.2:c.1867C>T	XP_006717351.1:p.His623Tyr
XM_011519021.1:c.1894C>T	XP_011517323.1:p.His632Tyr
XM_011519022.1:c.1891C>T	XP_011517324.1:p.His631Tyr
XM_011519023.1:c.1873C>T	XP_011517325.1:p.His625Tyr
XM_011519024.1:c.1816C>T	XP_011517326.1:p.His606Tyr
XM_011519025.1:c.1792C>T	XP_011517327.1:p.His598Tyr
XM_011519026.1:c.1750C>T	XP_011517328.1:p.His584Tyr
XM_011519027.1:c.1894C>T	XP_011517329.1:p.His632Tyr
XM_011519028.1:c.1894C>T	XP_011517330.1:p.His632Tyr
XM_011519029.1:c.316C>T	XP_011517331.1:p.His106Tyr
XM_011519033.1:c.1729C>T	XP_011517335.1:p.His577Tyr
NM_001354259.1:c.1792C>T	NP_001341188.1:p.His598Tyr
NM_001354263.1:c.1864C>T	NP_001341192.1:p.His622Tyr
XM_005266105.5:c.1876C>T	XP_005266162.1:p.His626Tyr
XM_011519021.3:c.1894C>T	XP_011517323.1:p.His632Tyr
XM_011519022.3:c.1891C>T	XP_011517324.1:p.His631Tyr
XM_011519023.3:c.1873C>T	XP_011517325.1:p.His625Tyr
XM_011519029.3:c.316C>T	XP_011517331.1:p.His106Tyr
XM_017015134.1:c.1870C>T	XP_016870623.1:p.His624Tyr
XM_017015136.2:c.1786C>T	XP_016870625.1:p.His596Tyr
XM_017015137.1:c.1771C>T	XP_016870626.1:p.His591Tyr
XM_017015138.1:c.1771C>T	XP_016870627.1:p.His591Tyr
XM_024447674.1:c.1714C>T	XP_024303442.1:p.His572Tyr
XM_024447675.1:c.1648C>T	XP_024303443.1:p.His550Tyr
XM_024447676.1:c.1009C>T	XP_024303444.1:p.His337Tyr
XM_024447677.1:c.1009C>T	XP_024303445.1:p.His337Tyr
XM_024447678.1:c.1792C>T	XP_024303446.1:p.His598Tyr
XM_024447679.1:c.1792C>T	XP_024303447.1:p.His598Tyr
XM_024447680.1:c.1627C>T	XP_024303448.1:p.His543Tyr
NM_024757.5:c.1885C>T MANE Select	NP_079033.4:p.His629Tyr
NM_001145527.2:c.1885C>T	NP_001138999.1:p.His629Tyr
NM_001354259.2:c.1792C>T	NP_001341188.1:p.His598Tyr
NM_001354263.2:c.1864C>T	NP_001341192.1:p.His622Tyr