Canonical Allele Identifier: CA467874152

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776821-C-T
• MyVariant Identifiers: chr9:g.140671273C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776821C>T , CM000671.2:g.137776821C>T	GRCh38
NC_000009.11:g.140671273C>T , CM000671.1:g.140671273C>T	GRCh37
NC_000009.10:g.139791094C>T	NCBI36
NG_011776.1:g.162830C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1995C>T MANE Select	ENSP00000417980.1:p.Gly665=
ENST00000636027.1:c.1881C>T	ENSP00000489961.1:p.Gly627=
ENST00000637161.1:c.1902C>T	ENSP00000490328.1:p.Gly634=
ENST00000637261.1:c.2035C>T	ENSP00000490815.1:n.2035C>T
ENST00000638071.1:c.1622C>T
ENST00000640639.1:c.1164C>T	ENSP00000491823.1:p.Gly388=
ENST00000371394.6:c.*1730C>T	ENSP00000485945.1:n.*1730C>T
ENST00000460843.5:c.1995C>T	ENSP00000417980.1:p.Gly665=
ENST00000462484.5:c.1995C>T	ENSP00000417328.1:p.Gly665=
ENST00000462942.3:c.852C>T	ENSP00000436107.1:p.Gly284=
ENST00000626603.1:n.1628G>A
NM_001145527.1:c.1995C>T	NP_001138999.1:p.Gly665=
NM_024757.4:c.1995C>T	NP_079033.4:p.Gly665=
XM_005266105.3:c.1986C>T	XP_005266162.1:p.Gly662=
XM_005266110.1:c.1902C>T	XP_005266167.1:p.Gly634=
XM_006717288.2:c.1977C>T	XP_006717351.1:p.Gly659=
XM_011519021.1:c.2004C>T	XP_011517323.1:p.Gly668=
XM_011519022.1:c.2001C>T	XP_011517324.1:p.Gly667=
XM_011519023.1:c.1983C>T	XP_011517325.1:p.Gly661=
XM_011519024.1:c.1926C>T	XP_011517326.1:p.Gly642=
XM_011519025.1:c.1902C>T	XP_011517327.1:p.Gly634=
XM_011519026.1:c.1860C>T	XP_011517328.1:p.Gly620=
XM_011519027.1:c.2004C>T	XP_011517329.1:p.Gly668=
XM_011519028.1:c.2004C>T	XP_011517330.1:p.Gly668=
XM_011519029.1:c.426C>T	XP_011517331.1:p.Gly142=
XM_011519033.1:c.1839C>T	XP_011517335.1:p.Gly613=
NM_001354259.1:c.1902C>T	NP_001341188.1:p.Gly634=
NM_001354263.1:c.1974C>T	NP_001341192.1:p.Gly658=
XM_005266105.5:c.1986C>T	XP_005266162.1:p.Gly662=
XM_011519021.3:c.2004C>T	XP_011517323.1:p.Gly668=
XM_011519022.3:c.2001C>T	XP_011517324.1:p.Gly667=
XM_011519023.3:c.1983C>T	XP_011517325.1:p.Gly661=
XM_011519029.3:c.426C>T	XP_011517331.1:p.Gly142=
XM_017015134.1:c.1980C>T	XP_016870623.1:p.Gly660=
XM_017015136.2:c.1896C>T	XP_016870625.1:p.Gly632=
XM_017015137.1:c.1881C>T	XP_016870626.1:p.Gly627=
XM_017015138.1:c.1881C>T	XP_016870627.1:p.Gly627=
XM_024447674.1:c.1824C>T	XP_024303442.1:p.Gly608=
XM_024447675.1:c.1758C>T	XP_024303443.1:p.Gly586=
XM_024447676.1:c.1119C>T	XP_024303444.1:p.Gly373=
XM_024447677.1:c.1119C>T	XP_024303445.1:p.Gly373=
XM_024447678.1:c.1902C>T	XP_024303446.1:p.Gly634=
XM_024447679.1:c.1902C>T	XP_024303447.1:p.Gly634=
XM_024447680.1:c.1737C>T	XP_024303448.1:p.Gly579=
NM_024757.5:c.1995C>T MANE Select	NP_079033.4:p.Gly665=
NM_001145527.2:c.1995C>T	NP_001138999.1:p.Gly665=
NM_001354259.2:c.1902C>T	NP_001341188.1:p.Gly634=
NM_001354263.2:c.1974C>T	NP_001341192.1:p.Gly658=