Canonical Allele Identifier: CA467874129

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671237A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776785A>G , CM000671.2:g.137776785A>G	GRCh38
NC_000009.11:g.140671237A>G , CM000671.1:g.140671237A>G	GRCh37
NC_000009.10:g.139791058A>G	NCBI36
NG_011776.1:g.162794A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1959A>G MANE Select	ENSP00000417980.1:p.Pro653=
ENST00000636027.1:c.1845A>G	ENSP00000489961.1:p.Pro615=
ENST00000637161.1:c.1866A>G	ENSP00000490328.1:p.Pro622=
ENST00000637261.1:c.1999A>G	ENSP00000490815.1:n.1999A>G
ENST00000638071.1:c.1586A>G
ENST00000640639.1:c.1128A>G	ENSP00000491823.1:p.Pro376=
ENST00000371394.6:c.*1694A>G	ENSP00000485945.1:n.*1694A>G
ENST00000460843.5:c.1959A>G	ENSP00000417980.1:p.Pro653=
ENST00000462484.5:c.1959A>G	ENSP00000417328.1:p.Pro653=
ENST00000462942.3:c.816A>G	ENSP00000436107.1:p.Pro272=
ENST00000626603.1:n.1664T>C
NM_001145527.1:c.1959A>G	NP_001138999.1:p.Pro653=
NM_024757.4:c.1959A>G	NP_079033.4:p.Pro653=
XM_005266105.3:c.1950A>G	XP_005266162.1:p.Pro650=
XM_005266110.1:c.1866A>G	XP_005266167.1:p.Pro622=
XM_006717288.2:c.1941A>G	XP_006717351.1:p.Pro647=
XM_011519021.1:c.1968A>G	XP_011517323.1:p.Pro656=
XM_011519022.1:c.1965A>G	XP_011517324.1:p.Pro655=
XM_011519023.1:c.1947A>G	XP_011517325.1:p.Pro649=
XM_011519024.1:c.1890A>G	XP_011517326.1:p.Pro630=
XM_011519025.1:c.1866A>G	XP_011517327.1:p.Pro622=
XM_011519026.1:c.1824A>G	XP_011517328.1:p.Pro608=
XM_011519027.1:c.1968A>G	XP_011517329.1:p.Pro656=
XM_011519028.1:c.1968A>G	XP_011517330.1:p.Pro656=
XM_011519029.1:c.390A>G	XP_011517331.1:p.Pro130=
XM_011519033.1:c.1803A>G	XP_011517335.1:p.Pro601=
NM_001354259.1:c.1866A>G	NP_001341188.1:p.Pro622=
NM_001354263.1:c.1938A>G	NP_001341192.1:p.Pro646=
XM_005266105.5:c.1950A>G	XP_005266162.1:p.Pro650=
XM_011519021.3:c.1968A>G	XP_011517323.1:p.Pro656=
XM_011519022.3:c.1965A>G	XP_011517324.1:p.Pro655=
XM_011519023.3:c.1947A>G	XP_011517325.1:p.Pro649=
XM_011519029.3:c.390A>G	XP_011517331.1:p.Pro130=
XM_017015134.1:c.1944A>G	XP_016870623.1:p.Pro648=
XM_017015136.2:c.1860A>G	XP_016870625.1:p.Pro620=
XM_017015137.1:c.1845A>G	XP_016870626.1:p.Pro615=
XM_017015138.1:c.1845A>G	XP_016870627.1:p.Pro615=
XM_024447674.1:c.1788A>G	XP_024303442.1:p.Pro596=
XM_024447675.1:c.1722A>G	XP_024303443.1:p.Pro574=
XM_024447676.1:c.1083A>G	XP_024303444.1:p.Pro361=
XM_024447677.1:c.1083A>G	XP_024303445.1:p.Pro361=
XM_024447678.1:c.1866A>G	XP_024303446.1:p.Pro622=
XM_024447679.1:c.1866A>G	XP_024303447.1:p.Pro622=
XM_024447680.1:c.1701A>G	XP_024303448.1:p.Pro567=
NM_024757.5:c.1959A>G MANE Select	NP_079033.4:p.Pro653=
NM_001145527.2:c.1959A>G	NP_001138999.1:p.Pro653=
NM_001354259.2:c.1866A>G	NP_001341188.1:p.Pro622=
NM_001354263.2:c.1938A>G	NP_001341192.1:p.Pro646=