Canonical Allele Identifier: CA467874156

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776824-G-A
• MyVariant Identifiers: chr9:g.140671276G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776824G>A , CM000671.2:g.137776824G>A	GRCh38
NC_000009.11:g.140671276G>A , CM000671.1:g.140671276G>A	GRCh37
NC_000009.10:g.139791097G>A	NCBI36
NG_011776.1:g.162833G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1998G>A MANE Select	ENSP00000417980.1:p.Arg666=
ENST00000636027.1:c.1884G>A	ENSP00000489961.1:p.Arg628=
ENST00000637161.1:c.1905G>A	ENSP00000490328.1:p.Arg635=
ENST00000637261.1:c.2038G>A	ENSP00000490815.1:n.2038G>A
ENST00000638071.1:c.1625G>A
ENST00000640639.1:c.1167G>A	ENSP00000491823.1:p.Arg389=
ENST00000371394.6:c.*1733G>A	ENSP00000485945.1:n.*1733G>A
ENST00000460843.5:c.1998G>A	ENSP00000417980.1:p.Arg666=
ENST00000462484.5:c.1998G>A	ENSP00000417328.1:p.Arg666=
ENST00000462942.3:c.855G>A	ENSP00000436107.1:p.Arg285=
ENST00000626603.1:n.1625C>T
NM_001145527.1:c.1998G>A	NP_001138999.1:p.Arg666=
NM_024757.4:c.1998G>A	NP_079033.4:p.Arg666=
XM_005266105.3:c.1989G>A	XP_005266162.1:p.Arg663=
XM_005266110.1:c.1905G>A	XP_005266167.1:p.Arg635=
XM_006717288.2:c.1980G>A	XP_006717351.1:p.Arg660=
XM_011519021.1:c.2007G>A	XP_011517323.1:p.Arg669=
XM_011519022.1:c.2004G>A	XP_011517324.1:p.Arg668=
XM_011519023.1:c.1986G>A	XP_011517325.1:p.Arg662=
XM_011519024.1:c.1929G>A	XP_011517326.1:p.Arg643=
XM_011519025.1:c.1905G>A	XP_011517327.1:p.Arg635=
XM_011519026.1:c.1863G>A	XP_011517328.1:p.Arg621=
XM_011519027.1:c.2007G>A	XP_011517329.1:p.Arg669=
XM_011519028.1:c.2007G>A	XP_011517330.1:p.Arg669=
XM_011519029.1:c.429G>A	XP_011517331.1:p.Arg143=
XM_011519033.1:c.1842G>A	XP_011517335.1:p.Arg614=
NM_001354259.1:c.1905G>A	NP_001341188.1:p.Arg635=
NM_001354263.1:c.1977G>A	NP_001341192.1:p.Arg659=
XM_005266105.5:c.1989G>A	XP_005266162.1:p.Arg663=
XM_011519021.3:c.2007G>A	XP_011517323.1:p.Arg669=
XM_011519022.3:c.2004G>A	XP_011517324.1:p.Arg668=
XM_011519023.3:c.1986G>A	XP_011517325.1:p.Arg662=
XM_011519029.3:c.429G>A	XP_011517331.1:p.Arg143=
XM_017015134.1:c.1983G>A	XP_016870623.1:p.Arg661=
XM_017015136.2:c.1899G>A	XP_016870625.1:p.Arg633=
XM_017015137.1:c.1884G>A	XP_016870626.1:p.Arg628=
XM_017015138.1:c.1884G>A	XP_016870627.1:p.Arg628=
XM_024447674.1:c.1827G>A	XP_024303442.1:p.Arg609=
XM_024447675.1:c.1761G>A	XP_024303443.1:p.Arg587=
XM_024447676.1:c.1122G>A	XP_024303444.1:p.Arg374=
XM_024447677.1:c.1122G>A	XP_024303445.1:p.Arg374=
XM_024447678.1:c.1905G>A	XP_024303446.1:p.Arg635=
XM_024447679.1:c.1905G>A	XP_024303447.1:p.Arg635=
XM_024447680.1:c.1740G>A	XP_024303448.1:p.Arg580=
NM_024757.5:c.1998G>A MANE Select	NP_079033.4:p.Arg666=
NM_001145527.2:c.1998G>A	NP_001138999.1:p.Arg666=
NM_001354259.2:c.1905G>A	NP_001341188.1:p.Arg635=
NM_001354263.2:c.1977G>A	NP_001341192.1:p.Arg659=