Canonical Allele Identifier: CA375776816

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671247C>G (hg19) ; chr9:g.137776795C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776795C>G , CM000671.2:g.137776795C>G	GRCh38
NC_000009.11:g.140671247C>G , CM000671.1:g.140671247C>G	GRCh37
NC_000009.10:g.139791068C>G	NCBI36
NG_011776.1:g.162804C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1969C>G MANE Select	ENSP00000417980.1:p.Gln657Glu
ENST00000636027.1:c.1855C>G	ENSP00000489961.1:p.Gln619Glu
ENST00000637161.1:c.1876C>G	ENSP00000490328.1:p.Gln626Glu
ENST00000637261.1:c.2009C>G	ENSP00000490815.1:n.2009C>G
ENST00000638071.1:c.1596C>G
ENST00000640639.1:c.1138C>G	ENSP00000491823.1:p.Gln380Glu
ENST00000371394.6:c.*1704C>G	ENSP00000485945.1:n.*1704C>G
ENST00000460843.5:c.1969C>G	ENSP00000417980.1:p.Gln657Glu
ENST00000462484.5:c.1969C>G	ENSP00000417328.1:p.Gln657Glu
ENST00000462942.3:c.826C>G	ENSP00000436107.1:p.Gln276Glu
ENST00000626603.1:n.1654G>C
NM_001145527.1:c.1969C>G	NP_001138999.1:p.Gln657Glu
NM_024757.4:c.1969C>G	NP_079033.4:p.Gln657Glu
XM_005266105.3:c.1960C>G	XP_005266162.1:p.Gln654Glu
XM_005266110.1:c.1876C>G	XP_005266167.1:p.Gln626Glu
XM_006717288.2:c.1951C>G	XP_006717351.1:p.Gln651Glu
XM_011519021.1:c.1978C>G	XP_011517323.1:p.Gln660Glu
XM_011519022.1:c.1975C>G	XP_011517324.1:p.Gln659Glu
XM_011519023.1:c.1957C>G	XP_011517325.1:p.Gln653Glu
XM_011519024.1:c.1900C>G	XP_011517326.1:p.Gln634Glu
XM_011519025.1:c.1876C>G	XP_011517327.1:p.Gln626Glu
XM_011519026.1:c.1834C>G	XP_011517328.1:p.Gln612Glu
XM_011519027.1:c.1978C>G	XP_011517329.1:p.Gln660Glu
XM_011519028.1:c.1978C>G	XP_011517330.1:p.Gln660Glu
XM_011519029.1:c.400C>G	XP_011517331.1:p.Gln134Glu
XM_011519033.1:c.1813C>G	XP_011517335.1:p.Gln605Glu
NM_001354259.1:c.1876C>G	NP_001341188.1:p.Gln626Glu
NM_001354263.1:c.1948C>G	NP_001341192.1:p.Gln650Glu
XM_005266105.5:c.1960C>G	XP_005266162.1:p.Gln654Glu
XM_011519021.3:c.1978C>G	XP_011517323.1:p.Gln660Glu
XM_011519022.3:c.1975C>G	XP_011517324.1:p.Gln659Glu
XM_011519023.3:c.1957C>G	XP_011517325.1:p.Gln653Glu
XM_011519029.3:c.400C>G	XP_011517331.1:p.Gln134Glu
XM_017015134.1:c.1954C>G	XP_016870623.1:p.Gln652Glu
XM_017015136.2:c.1870C>G	XP_016870625.1:p.Gln624Glu
XM_017015137.1:c.1855C>G	XP_016870626.1:p.Gln619Glu
XM_017015138.1:c.1855C>G	XP_016870627.1:p.Gln619Glu
XM_024447674.1:c.1798C>G	XP_024303442.1:p.Gln600Glu
XM_024447675.1:c.1732C>G	XP_024303443.1:p.Gln578Glu
XM_024447676.1:c.1093C>G	XP_024303444.1:p.Gln365Glu
XM_024447677.1:c.1093C>G	XP_024303445.1:p.Gln365Glu
XM_024447678.1:c.1876C>G	XP_024303446.1:p.Gln626Glu
XM_024447679.1:c.1876C>G	XP_024303447.1:p.Gln626Glu
XM_024447680.1:c.1711C>G	XP_024303448.1:p.Gln571Glu
NM_024757.5:c.1969C>G MANE Select	NP_079033.4:p.Gln657Glu
NM_001145527.2:c.1969C>G	NP_001138999.1:p.Gln657Glu
NM_001354259.2:c.1876C>G	NP_001341188.1:p.Gln626Glu
NM_001354263.2:c.1948C>G	NP_001341192.1:p.Gln650Glu