Canonical Allele Identifier: CA1884666530

Gene: EHMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776831A= , CM000671.2:g.137776831A=	GRCh38
NC_000009.11:g.140671283A= , CM000671.1:g.140671283A=	GRCh37
NC_000009.10:g.139791104A=	NCBI36
NG_011776.1:g.162840A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2005A= MANE Select	ENSP00000417980.1:p.Thr669=
ENST00000636027.1:c.1891A=	ENSP00000489961.1:p.Thr631=
ENST00000637161.1:c.1912A=	ENSP00000490328.1:p.Thr638=
ENST00000637261.1:c.2045A=	ENSP00000490815.1:n.2045A=
ENST00000638071.1:c.1632A=
ENST00000640639.1:c.1174A=	ENSP00000491823.1:p.Thr392=
ENST00000371394.6:c.*1740A=	ENSP00000485945.1:n.*1740A=
ENST00000460843.5:c.2005A=	ENSP00000417980.1:p.Thr669=
ENST00000462484.5:c.2005A=	ENSP00000417328.1:p.Thr669=
ENST00000462942.3:c.862A=	ENSP00000436107.1:p.Thr288=
ENST00000626603.1:n.1618T=
NM_001145527.1:c.2005A=	NP_001138999.1:p.Thr669=
NM_024757.4:c.2005A=	NP_079033.4:p.Thr669=
XM_005266105.3:c.1996A=	XP_005266162.1:p.Thr666=
XM_005266110.1:c.1912A=	XP_005266167.1:p.Thr638=
XM_006717288.2:c.1987A=	XP_006717351.1:p.Thr663=
XM_011519021.1:c.2014A=	XP_011517323.1:p.Thr672=
XM_011519022.1:c.2011A=	XP_011517324.1:p.Thr671=
XM_011519023.1:c.1993A=	XP_011517325.1:p.Thr665=
XM_011519024.1:c.1936A=	XP_011517326.1:p.Thr646=
XM_011519025.1:c.1912A=	XP_011517327.1:p.Thr638=
XM_011519026.1:c.1870A=	XP_011517328.1:p.Thr624=
XM_011519027.1:c.2014A=	XP_011517329.1:p.Thr672=
XM_011519028.1:c.2014A=	XP_011517330.1:p.Thr672=
XM_011519029.1:c.436A=	XP_011517331.1:p.Thr146=
XM_011519033.1:c.1849A=	XP_011517335.1:p.Thr617=
NM_001354259.1:c.1912A=	NP_001341188.1:p.Thr638=
NM_001354263.1:c.1984A=	NP_001341192.1:p.Thr662=
XM_005266105.5:c.1996A=	XP_005266162.1:p.Thr666=
XM_011519021.3:c.2014A=	XP_011517323.1:p.Thr672=
XM_011519022.3:c.2011A=	XP_011517324.1:p.Thr671=
XM_011519023.3:c.1993A=	XP_011517325.1:p.Thr665=
XM_011519029.3:c.436A=	XP_011517331.1:p.Thr146=
XM_017015134.1:c.1990A=	XP_016870623.1:p.Thr664=
XM_017015136.2:c.1906A=	XP_016870625.1:p.Thr636=
XM_017015137.1:c.1891A=	XP_016870626.1:p.Thr631=
XM_017015138.1:c.1891A=	XP_016870627.1:p.Thr631=
XM_024447674.1:c.1834A=	XP_024303442.1:p.Thr612=
XM_024447675.1:c.1768A=	XP_024303443.1:p.Thr590=
XM_024447676.1:c.1129A=	XP_024303444.1:p.Thr377=
XM_024447677.1:c.1129A=	XP_024303445.1:p.Thr377=
XM_024447678.1:c.1912A=	XP_024303446.1:p.Thr638=
XM_024447679.1:c.1912A=	XP_024303447.1:p.Thr638=
XM_024447680.1:c.1747A=	XP_024303448.1:p.Thr583=
NM_024757.5:c.2005A= MANE Select	NP_079033.4:p.Thr669=
NM_001145527.2:c.2005A=	NP_001138999.1:p.Thr669=
NM_001354259.2:c.1912A=	NP_001341188.1:p.Thr638=
NM_001354263.2:c.1984A=	NP_001341192.1:p.Thr662=