Canonical Allele Identifier: CA375775874

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671121A>T (hg19) ; chr9:g.137776669A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776669A>T , CM000671.2:g.137776669A>T	GRCh38
NC_000009.11:g.140671121A>T , CM000671.1:g.140671121A>T	GRCh37
NC_000009.10:g.139790942A>T	NCBI36
NG_011776.1:g.162678A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1843A>T MANE Select	ENSP00000417980.1:p.Lys615Ter
ENST00000636027.1:c.1729A>T	ENSP00000489961.1:p.Lys577Ter
ENST00000637161.1:c.1750A>T	ENSP00000490328.1:p.Lys584Ter
ENST00000637261.1:c.1883A>T	ENSP00000490815.1:n.1883A>T
ENST00000638071.1:c.1470A>T
ENST00000640639.1:c.1012A>T	ENSP00000491823.1:p.Lys338Ter
ENST00000371394.6:c.*1578A>T	ENSP00000485945.1:n.*1578A>T
ENST00000460843.5:c.1843A>T	ENSP00000417980.1:p.Lys615Ter
ENST00000462484.5:c.1843A>T	ENSP00000417328.1:p.Lys615Ter
ENST00000462942.3:c.700A>T	ENSP00000436107.1:p.Lys234Ter
ENST00000465566.2:c.391A>T	ENSP00000486261.1:p.Lys131Ter
ENST00000626603.1:n.1780T>A
NM_001145527.1:c.1843A>T	NP_001138999.1:p.Lys615Ter
NM_024757.4:c.1843A>T	NP_079033.4:p.Lys615Ter
XM_005266105.3:c.1834A>T	XP_005266162.1:p.Lys612Ter
XM_005266110.1:c.1750A>T	XP_005266167.1:p.Lys584Ter
XM_006717288.2:c.1825A>T	XP_006717351.1:p.Lys609Ter
XM_011519021.1:c.1852A>T	XP_011517323.1:p.Lys618Ter
XM_011519022.1:c.1849A>T	XP_011517324.1:p.Lys617Ter
XM_011519023.1:c.1831A>T	XP_011517325.1:p.Lys611Ter
XM_011519024.1:c.1774A>T	XP_011517326.1:p.Lys592Ter
XM_011519025.1:c.1750A>T	XP_011517327.1:p.Lys584Ter
XM_011519026.1:c.1708A>T	XP_011517328.1:p.Lys570Ter
XM_011519027.1:c.1852A>T	XP_011517329.1:p.Lys618Ter
XM_011519028.1:c.1852A>T	XP_011517330.1:p.Lys618Ter
XM_011519029.1:c.274A>T	XP_011517331.1:p.Lys92Ter
XM_011519033.1:c.1687A>T	XP_011517335.1:p.Lys563Ter
NM_001354259.1:c.1750A>T	NP_001341188.1:p.Lys584Ter
NM_001354263.1:c.1822A>T	NP_001341192.1:p.Lys608Ter
XM_005266105.5:c.1834A>T	XP_005266162.1:p.Lys612Ter
XM_011519021.3:c.1852A>T	XP_011517323.1:p.Lys618Ter
XM_011519022.3:c.1849A>T	XP_011517324.1:p.Lys617Ter
XM_011519023.3:c.1831A>T	XP_011517325.1:p.Lys611Ter
XM_011519029.3:c.274A>T	XP_011517331.1:p.Lys92Ter
XM_017015134.1:c.1828A>T	XP_016870623.1:p.Lys610Ter
XM_017015136.2:c.1744A>T	XP_016870625.1:p.Lys582Ter
XM_017015137.1:c.1729A>T	XP_016870626.1:p.Lys577Ter
XM_017015138.1:c.1729A>T	XP_016870627.1:p.Lys577Ter
XM_024447674.1:c.1672A>T	XP_024303442.1:p.Lys558Ter
XM_024447675.1:c.1606A>T	XP_024303443.1:p.Lys536Ter
XM_024447676.1:c.967A>T	XP_024303444.1:p.Lys323Ter
XM_024447677.1:c.967A>T	XP_024303445.1:p.Lys323Ter
XM_024447678.1:c.1750A>T	XP_024303446.1:p.Lys584Ter
XM_024447679.1:c.1750A>T	XP_024303447.1:p.Lys584Ter
XM_024447680.1:c.1585A>T	XP_024303448.1:p.Lys529Ter
NM_024757.5:c.1843A>T MANE Select	NP_079033.4:p.Lys615Ter
NM_001145527.2:c.1843A>T	NP_001138999.1:p.Lys615Ter
NM_001354259.2:c.1750A>T	NP_001341188.1:p.Lys584Ter
NM_001354263.2:c.1822A>T	NP_001341192.1:p.Lys608Ter