Canonical Allele Identifier: CA375776543

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671202A>G (hg19) ; chr9:g.137776750A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776750A>G , CM000671.2:g.137776750A>G	GRCh38
NC_000009.11:g.140671202A>G , CM000671.1:g.140671202A>G	GRCh37
NC_000009.10:g.139791023A>G	NCBI36
NG_011776.1:g.162759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1924A>G MANE Select	ENSP00000417980.1:p.Ile642Val
ENST00000636027.1:c.1810A>G	ENSP00000489961.1:p.Ile604Val
ENST00000637161.1:c.1831A>G	ENSP00000490328.1:p.Ile611Val
ENST00000637261.1:c.1964A>G	ENSP00000490815.1:n.1964A>G
ENST00000638071.1:c.1551A>G
ENST00000640639.1:c.1093A>G	ENSP00000491823.1:p.Ile365Val
ENST00000371394.6:c.*1659A>G	ENSP00000485945.1:n.*1659A>G
ENST00000460843.5:c.1924A>G	ENSP00000417980.1:p.Ile642Val
ENST00000462484.5:c.1924A>G	ENSP00000417328.1:p.Ile642Val
ENST00000462942.3:c.781A>G	ENSP00000436107.1:p.Ile261Val
ENST00000465566.2:c.472A>G	ENSP00000486261.1:p.Ile158Val
ENST00000626603.1:n.1699T>C
NM_001145527.1:c.1924A>G	NP_001138999.1:p.Ile642Val
NM_024757.4:c.1924A>G	NP_079033.4:p.Ile642Val
XM_005266105.3:c.1915A>G	XP_005266162.1:p.Ile639Val
XM_005266110.1:c.1831A>G	XP_005266167.1:p.Ile611Val
XM_006717288.2:c.1906A>G	XP_006717351.1:p.Ile636Val
XM_011519021.1:c.1933A>G	XP_011517323.1:p.Ile645Val
XM_011519022.1:c.1930A>G	XP_011517324.1:p.Ile644Val
XM_011519023.1:c.1912A>G	XP_011517325.1:p.Ile638Val
XM_011519024.1:c.1855A>G	XP_011517326.1:p.Ile619Val
XM_011519025.1:c.1831A>G	XP_011517327.1:p.Ile611Val
XM_011519026.1:c.1789A>G	XP_011517328.1:p.Ile597Val
XM_011519027.1:c.1933A>G	XP_011517329.1:p.Ile645Val
XM_011519028.1:c.1933A>G	XP_011517330.1:p.Ile645Val
XM_011519029.1:c.355A>G	XP_011517331.1:p.Ile119Val
XM_011519033.1:c.1768A>G	XP_011517335.1:p.Ile590Val
NM_001354259.1:c.1831A>G	NP_001341188.1:p.Ile611Val
NM_001354263.1:c.1903A>G	NP_001341192.1:p.Ile635Val
XM_005266105.5:c.1915A>G	XP_005266162.1:p.Ile639Val
XM_011519021.3:c.1933A>G	XP_011517323.1:p.Ile645Val
XM_011519022.3:c.1930A>G	XP_011517324.1:p.Ile644Val
XM_011519023.3:c.1912A>G	XP_011517325.1:p.Ile638Val
XM_011519029.3:c.355A>G	XP_011517331.1:p.Ile119Val
XM_017015134.1:c.1909A>G	XP_016870623.1:p.Ile637Val
XM_017015136.2:c.1825A>G	XP_016870625.1:p.Ile609Val
XM_017015137.1:c.1810A>G	XP_016870626.1:p.Ile604Val
XM_017015138.1:c.1810A>G	XP_016870627.1:p.Ile604Val
XM_024447674.1:c.1753A>G	XP_024303442.1:p.Ile585Val
XM_024447675.1:c.1687A>G	XP_024303443.1:p.Ile563Val
XM_024447676.1:c.1048A>G	XP_024303444.1:p.Ile350Val
XM_024447677.1:c.1048A>G	XP_024303445.1:p.Ile350Val
XM_024447678.1:c.1831A>G	XP_024303446.1:p.Ile611Val
XM_024447679.1:c.1831A>G	XP_024303447.1:p.Ile611Val
XM_024447680.1:c.1666A>G	XP_024303448.1:p.Ile556Val
NM_024757.5:c.1924A>G MANE Select	NP_079033.4:p.Ile642Val
NM_001145527.2:c.1924A>G	NP_001138999.1:p.Ile642Val
NM_001354259.2:c.1831A>G	NP_001341188.1:p.Ile611Val
NM_001354263.2:c.1903A>G	NP_001341192.1:p.Ile635Val