Canonical Allele Identifier: CA467874070

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671141C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776689C>A , CM000671.2:g.137776689C>A	GRCh38
NC_000009.11:g.140671141C>A , CM000671.1:g.140671141C>A	GRCh37
NC_000009.10:g.139790962C>A	NCBI36
NG_011776.1:g.162698C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1863C>A MANE Select	ENSP00000417980.1:p.Val621=
ENST00000636027.1:c.1749C>A	ENSP00000489961.1:p.Val583=
ENST00000637161.1:c.1770C>A	ENSP00000490328.1:p.Val590=
ENST00000637261.1:c.1903C>A	ENSP00000490815.1:n.1903C>A
ENST00000638071.1:c.1490C>A
ENST00000640639.1:c.1032C>A	ENSP00000491823.1:p.Val344=
ENST00000371394.6:c.*1598C>A	ENSP00000485945.1:n.*1598C>A
ENST00000460843.5:c.1863C>A	ENSP00000417980.1:p.Val621=
ENST00000462484.5:c.1863C>A	ENSP00000417328.1:p.Val621=
ENST00000462942.3:c.720C>A	ENSP00000436107.1:p.Val240=
ENST00000465566.2:c.411C>A	ENSP00000486261.1:p.Val137=
ENST00000626603.1:n.1760G>T
NM_001145527.1:c.1863C>A	NP_001138999.1:p.Val621=
NM_024757.4:c.1863C>A	NP_079033.4:p.Val621=
XM_005266105.3:c.1854C>A	XP_005266162.1:p.Val618=
XM_005266110.1:c.1770C>A	XP_005266167.1:p.Val590=
XM_006717288.2:c.1845C>A	XP_006717351.1:p.Val615=
XM_011519021.1:c.1872C>A	XP_011517323.1:p.Val624=
XM_011519022.1:c.1869C>A	XP_011517324.1:p.Val623=
XM_011519023.1:c.1851C>A	XP_011517325.1:p.Val617=
XM_011519024.1:c.1794C>A	XP_011517326.1:p.Val598=
XM_011519025.1:c.1770C>A	XP_011517327.1:p.Val590=
XM_011519026.1:c.1728C>A	XP_011517328.1:p.Val576=
XM_011519027.1:c.1872C>A	XP_011517329.1:p.Val624=
XM_011519028.1:c.1872C>A	XP_011517330.1:p.Val624=
XM_011519029.1:c.294C>A	XP_011517331.1:p.Val98=
XM_011519033.1:c.1707C>A	XP_011517335.1:p.Val569=
NM_001354259.1:c.1770C>A	NP_001341188.1:p.Val590=
NM_001354263.1:c.1842C>A	NP_001341192.1:p.Val614=
XM_005266105.5:c.1854C>A	XP_005266162.1:p.Val618=
XM_011519021.3:c.1872C>A	XP_011517323.1:p.Val624=
XM_011519022.3:c.1869C>A	XP_011517324.1:p.Val623=
XM_011519023.3:c.1851C>A	XP_011517325.1:p.Val617=
XM_011519029.3:c.294C>A	XP_011517331.1:p.Val98=
XM_017015134.1:c.1848C>A	XP_016870623.1:p.Val616=
XM_017015136.2:c.1764C>A	XP_016870625.1:p.Val588=
XM_017015137.1:c.1749C>A	XP_016870626.1:p.Val583=
XM_017015138.1:c.1749C>A	XP_016870627.1:p.Val583=
XM_024447674.1:c.1692C>A	XP_024303442.1:p.Val564=
XM_024447675.1:c.1626C>A	XP_024303443.1:p.Val542=
XM_024447676.1:c.987C>A	XP_024303444.1:p.Val329=
XM_024447677.1:c.987C>A	XP_024303445.1:p.Val329=
XM_024447678.1:c.1770C>A	XP_024303446.1:p.Val590=
XM_024447679.1:c.1770C>A	XP_024303447.1:p.Val590=
XM_024447680.1:c.1605C>A	XP_024303448.1:p.Val535=
NM_024757.5:c.1863C>A MANE Select	NP_079033.4:p.Val621=
NM_001145527.2:c.1863C>A	NP_001138999.1:p.Val621=
NM_001354259.2:c.1770C>A	NP_001341188.1:p.Val590=
NM_001354263.2:c.1842C>A	NP_001341192.1:p.Val614=