Canonical Allele Identifier: CA375776304

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671175G>C (hg19) ; chr9:g.137776723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776723G>C , CM000671.2:g.137776723G>C	GRCh38
NC_000009.11:g.140671175G>C , CM000671.1:g.140671175G>C	GRCh37
NC_000009.10:g.139790996G>C	NCBI36
NG_011776.1:g.162732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1897G>C MANE Select	ENSP00000417980.1:p.Glu633Gln
ENST00000636027.1:c.1783G>C	ENSP00000489961.1:p.Glu595Gln
ENST00000637161.1:c.1804G>C	ENSP00000490328.1:p.Glu602Gln
ENST00000637261.1:c.1937G>C	ENSP00000490815.1:n.1937G>C
ENST00000638071.1:c.1524G>C
ENST00000640639.1:c.1066G>C	ENSP00000491823.1:p.Glu356Gln
ENST00000371394.6:c.*1632G>C	ENSP00000485945.1:n.*1632G>C
ENST00000460843.5:c.1897G>C	ENSP00000417980.1:p.Glu633Gln
ENST00000462484.5:c.1897G>C	ENSP00000417328.1:p.Glu633Gln
ENST00000462942.3:c.754G>C	ENSP00000436107.1:p.Glu252Gln
ENST00000465566.2:c.445G>C	ENSP00000486261.1:p.Glu149Gln
ENST00000626603.1:n.1726C>G
NM_001145527.1:c.1897G>C	NP_001138999.1:p.Glu633Gln
NM_024757.4:c.1897G>C	NP_079033.4:p.Glu633Gln
XM_005266105.3:c.1888G>C	XP_005266162.1:p.Glu630Gln
XM_005266110.1:c.1804G>C	XP_005266167.1:p.Glu602Gln
XM_006717288.2:c.1879G>C	XP_006717351.1:p.Glu627Gln
XM_011519021.1:c.1906G>C	XP_011517323.1:p.Glu636Gln
XM_011519022.1:c.1903G>C	XP_011517324.1:p.Glu635Gln
XM_011519023.1:c.1885G>C	XP_011517325.1:p.Glu629Gln
XM_011519024.1:c.1828G>C	XP_011517326.1:p.Glu610Gln
XM_011519025.1:c.1804G>C	XP_011517327.1:p.Glu602Gln
XM_011519026.1:c.1762G>C	XP_011517328.1:p.Glu588Gln
XM_011519027.1:c.1906G>C	XP_011517329.1:p.Glu636Gln
XM_011519028.1:c.1906G>C	XP_011517330.1:p.Glu636Gln
XM_011519029.1:c.328G>C	XP_011517331.1:p.Glu110Gln
XM_011519033.1:c.1741G>C	XP_011517335.1:p.Glu581Gln
NM_001354259.1:c.1804G>C	NP_001341188.1:p.Glu602Gln
NM_001354263.1:c.1876G>C	NP_001341192.1:p.Glu626Gln
XM_005266105.5:c.1888G>C	XP_005266162.1:p.Glu630Gln
XM_011519021.3:c.1906G>C	XP_011517323.1:p.Glu636Gln
XM_011519022.3:c.1903G>C	XP_011517324.1:p.Glu635Gln
XM_011519023.3:c.1885G>C	XP_011517325.1:p.Glu629Gln
XM_011519029.3:c.328G>C	XP_011517331.1:p.Glu110Gln
XM_017015134.1:c.1882G>C	XP_016870623.1:p.Glu628Gln
XM_017015136.2:c.1798G>C	XP_016870625.1:p.Glu600Gln
XM_017015137.1:c.1783G>C	XP_016870626.1:p.Glu595Gln
XM_017015138.1:c.1783G>C	XP_016870627.1:p.Glu595Gln
XM_024447674.1:c.1726G>C	XP_024303442.1:p.Glu576Gln
XM_024447675.1:c.1660G>C	XP_024303443.1:p.Glu554Gln
XM_024447676.1:c.1021G>C	XP_024303444.1:p.Glu341Gln
XM_024447677.1:c.1021G>C	XP_024303445.1:p.Glu341Gln
XM_024447678.1:c.1804G>C	XP_024303446.1:p.Glu602Gln
XM_024447679.1:c.1804G>C	XP_024303447.1:p.Glu602Gln
XM_024447680.1:c.1639G>C	XP_024303448.1:p.Glu547Gln
NM_024757.5:c.1897G>C MANE Select	NP_079033.4:p.Glu633Gln
NM_001145527.2:c.1897G>C	NP_001138999.1:p.Glu633Gln
NM_001354259.2:c.1804G>C	NP_001341188.1:p.Glu602Gln
NM_001354263.2:c.1876G>C	NP_001341192.1:p.Glu626Gln