Canonical Allele Identifier: CA375776690

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671223T>A (hg19) ; chr9:g.137776771T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776771T>A , CM000671.2:g.137776771T>A	GRCh38
NC_000009.11:g.140671223T>A , CM000671.1:g.140671223T>A	GRCh37
NC_000009.10:g.139791044T>A	NCBI36
NG_011776.1:g.162780T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1945T>A MANE Select	ENSP00000417980.1:p.Ser649Thr
ENST00000636027.1:c.1831T>A	ENSP00000489961.1:p.Ser611Thr
ENST00000637161.1:c.1852T>A	ENSP00000490328.1:p.Ser618Thr
ENST00000637261.1:c.1985T>A	ENSP00000490815.1:n.1985T>A
ENST00000638071.1:c.1572T>A
ENST00000640639.1:c.1114T>A	ENSP00000491823.1:p.Ser372Thr
ENST00000371394.6:c.*1680T>A	ENSP00000485945.1:n.*1680T>A
ENST00000460843.5:c.1945T>A	ENSP00000417980.1:p.Ser649Thr
ENST00000462484.5:c.1945T>A	ENSP00000417328.1:p.Ser649Thr
ENST00000462942.3:c.802T>A	ENSP00000436107.1:p.Ser268Thr
ENST00000465566.2:c.493T>A	ENSP00000486261.1:p.Ser165Thr
ENST00000626603.1:n.1678A>T
NM_001145527.1:c.1945T>A	NP_001138999.1:p.Ser649Thr
NM_024757.4:c.1945T>A	NP_079033.4:p.Ser649Thr
XM_005266105.3:c.1936T>A	XP_005266162.1:p.Ser646Thr
XM_005266110.1:c.1852T>A	XP_005266167.1:p.Ser618Thr
XM_006717288.2:c.1927T>A	XP_006717351.1:p.Ser643Thr
XM_011519021.1:c.1954T>A	XP_011517323.1:p.Ser652Thr
XM_011519022.1:c.1951T>A	XP_011517324.1:p.Ser651Thr
XM_011519023.1:c.1933T>A	XP_011517325.1:p.Ser645Thr
XM_011519024.1:c.1876T>A	XP_011517326.1:p.Ser626Thr
XM_011519025.1:c.1852T>A	XP_011517327.1:p.Ser618Thr
XM_011519026.1:c.1810T>A	XP_011517328.1:p.Ser604Thr
XM_011519027.1:c.1954T>A	XP_011517329.1:p.Ser652Thr
XM_011519028.1:c.1954T>A	XP_011517330.1:p.Ser652Thr
XM_011519029.1:c.376T>A	XP_011517331.1:p.Ser126Thr
XM_011519033.1:c.1789T>A	XP_011517335.1:p.Ser597Thr
NM_001354259.1:c.1852T>A	NP_001341188.1:p.Ser618Thr
NM_001354263.1:c.1924T>A	NP_001341192.1:p.Ser642Thr
XM_005266105.5:c.1936T>A	XP_005266162.1:p.Ser646Thr
XM_011519021.3:c.1954T>A	XP_011517323.1:p.Ser652Thr
XM_011519022.3:c.1951T>A	XP_011517324.1:p.Ser651Thr
XM_011519023.3:c.1933T>A	XP_011517325.1:p.Ser645Thr
XM_011519029.3:c.376T>A	XP_011517331.1:p.Ser126Thr
XM_017015134.1:c.1930T>A	XP_016870623.1:p.Ser644Thr
XM_017015136.2:c.1846T>A	XP_016870625.1:p.Ser616Thr
XM_017015137.1:c.1831T>A	XP_016870626.1:p.Ser611Thr
XM_017015138.1:c.1831T>A	XP_016870627.1:p.Ser611Thr
XM_024447674.1:c.1774T>A	XP_024303442.1:p.Ser592Thr
XM_024447675.1:c.1708T>A	XP_024303443.1:p.Ser570Thr
XM_024447676.1:c.1069T>A	XP_024303444.1:p.Ser357Thr
XM_024447677.1:c.1069T>A	XP_024303445.1:p.Ser357Thr
XM_024447678.1:c.1852T>A	XP_024303446.1:p.Ser618Thr
XM_024447679.1:c.1852T>A	XP_024303447.1:p.Ser618Thr
XM_024447680.1:c.1687T>A	XP_024303448.1:p.Ser563Thr
NM_024757.5:c.1945T>A MANE Select	NP_079033.4:p.Ser649Thr
NM_001145527.2:c.1945T>A	NP_001138999.1:p.Ser649Thr
NM_001354259.2:c.1852T>A	NP_001341188.1:p.Ser618Thr
NM_001354263.2:c.1924T>A	NP_001341192.1:p.Ser642Thr