Canonical Allele Identifier: CA467874110

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671213A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776761A>T , CM000671.2:g.137776761A>T	GRCh38
NC_000009.11:g.140671213A>T , CM000671.1:g.140671213A>T	GRCh37
NC_000009.10:g.139791034A>T	NCBI36
NG_011776.1:g.162770A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1935A>T MANE Select	ENSP00000417980.1:p.Ala645=
ENST00000636027.1:c.1821A>T	ENSP00000489961.1:p.Ala607=
ENST00000637161.1:c.1842A>T	ENSP00000490328.1:p.Ala614=
ENST00000637261.1:c.1975A>T	ENSP00000490815.1:n.1975A>T
ENST00000638071.1:c.1562A>T
ENST00000640639.1:c.1104A>T	ENSP00000491823.1:p.Ala368=
ENST00000371394.6:c.*1670A>T	ENSP00000485945.1:n.*1670A>T
ENST00000460843.5:c.1935A>T	ENSP00000417980.1:p.Ala645=
ENST00000462484.5:c.1935A>T	ENSP00000417328.1:p.Ala645=
ENST00000462942.3:c.792A>T	ENSP00000436107.1:p.Ala264=
ENST00000465566.2:c.483A>T	ENSP00000486261.1:p.Ala161=
ENST00000626603.1:n.1688T>A
NM_001145527.1:c.1935A>T	NP_001138999.1:p.Ala645=
NM_024757.4:c.1935A>T	NP_079033.4:p.Ala645=
XM_005266105.3:c.1926A>T	XP_005266162.1:p.Ala642=
XM_005266110.1:c.1842A>T	XP_005266167.1:p.Ala614=
XM_006717288.2:c.1917A>T	XP_006717351.1:p.Ala639=
XM_011519021.1:c.1944A>T	XP_011517323.1:p.Ala648=
XM_011519022.1:c.1941A>T	XP_011517324.1:p.Ala647=
XM_011519023.1:c.1923A>T	XP_011517325.1:p.Ala641=
XM_011519024.1:c.1866A>T	XP_011517326.1:p.Ala622=
XM_011519025.1:c.1842A>T	XP_011517327.1:p.Ala614=
XM_011519026.1:c.1800A>T	XP_011517328.1:p.Ala600=
XM_011519027.1:c.1944A>T	XP_011517329.1:p.Ala648=
XM_011519028.1:c.1944A>T	XP_011517330.1:p.Ala648=
XM_011519029.1:c.366A>T	XP_011517331.1:p.Ala122=
XM_011519033.1:c.1779A>T	XP_011517335.1:p.Ala593=
NM_001354259.1:c.1842A>T	NP_001341188.1:p.Ala614=
NM_001354263.1:c.1914A>T	NP_001341192.1:p.Ala638=
XM_005266105.5:c.1926A>T	XP_005266162.1:p.Ala642=
XM_011519021.3:c.1944A>T	XP_011517323.1:p.Ala648=
XM_011519022.3:c.1941A>T	XP_011517324.1:p.Ala647=
XM_011519023.3:c.1923A>T	XP_011517325.1:p.Ala641=
XM_011519029.3:c.366A>T	XP_011517331.1:p.Ala122=
XM_017015134.1:c.1920A>T	XP_016870623.1:p.Ala640=
XM_017015136.2:c.1836A>T	XP_016870625.1:p.Ala612=
XM_017015137.1:c.1821A>T	XP_016870626.1:p.Ala607=
XM_017015138.1:c.1821A>T	XP_016870627.1:p.Ala607=
XM_024447674.1:c.1764A>T	XP_024303442.1:p.Ala588=
XM_024447675.1:c.1698A>T	XP_024303443.1:p.Ala566=
XM_024447676.1:c.1059A>T	XP_024303444.1:p.Ala353=
XM_024447677.1:c.1059A>T	XP_024303445.1:p.Ala353=
XM_024447678.1:c.1842A>T	XP_024303446.1:p.Ala614=
XM_024447679.1:c.1842A>T	XP_024303447.1:p.Ala614=
XM_024447680.1:c.1677A>T	XP_024303448.1:p.Ala559=
NM_024757.5:c.1935A>T MANE Select	NP_079033.4:p.Ala645=
NM_001145527.2:c.1935A>T	NP_001138999.1:p.Ala645=
NM_001354259.2:c.1842A>T	NP_001341188.1:p.Ala614=
NM_001354263.2:c.1914A>T	NP_001341192.1:p.Ala638=