Canonical Allele Identifier: CA375776900

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671260C>A (hg19) ; chr9:g.137776808C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776808C>A , CM000671.2:g.137776808C>A	GRCh38
NC_000009.11:g.140671260C>A , CM000671.1:g.140671260C>A	GRCh37
NC_000009.10:g.139791081C>A	NCBI36
NG_011776.1:g.162817C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1982C>A MANE Select	ENSP00000417980.1:p.Ser661Ter
ENST00000636027.1:c.1868C>A	ENSP00000489961.1:p.Ser623Ter
ENST00000637161.1:c.1889C>A	ENSP00000490328.1:p.Ser630Ter
ENST00000637261.1:c.2022C>A	ENSP00000490815.1:n.2022C>A
ENST00000638071.1:c.1609C>A
ENST00000640639.1:c.1151C>A	ENSP00000491823.1:p.Ser384Ter
ENST00000371394.6:c.*1717C>A	ENSP00000485945.1:n.*1717C>A
ENST00000460843.5:c.1982C>A	ENSP00000417980.1:p.Ser661Ter
ENST00000462484.5:c.1982C>A	ENSP00000417328.1:p.Ser661Ter
ENST00000462942.3:c.839C>A	ENSP00000436107.1:p.Ser280Ter
ENST00000626603.1:n.1641G>T
NM_001145527.1:c.1982C>A	NP_001138999.1:p.Ser661Ter
NM_024757.4:c.1982C>A	NP_079033.4:p.Ser661Ter
XM_005266105.3:c.1973C>A	XP_005266162.1:p.Ser658Ter
XM_005266110.1:c.1889C>A	XP_005266167.1:p.Ser630Ter
XM_006717288.2:c.1964C>A	XP_006717351.1:p.Ser655Ter
XM_011519021.1:c.1991C>A	XP_011517323.1:p.Ser664Ter
XM_011519022.1:c.1988C>A	XP_011517324.1:p.Ser663Ter
XM_011519023.1:c.1970C>A	XP_011517325.1:p.Ser657Ter
XM_011519024.1:c.1913C>A	XP_011517326.1:p.Ser638Ter
XM_011519025.1:c.1889C>A	XP_011517327.1:p.Ser630Ter
XM_011519026.1:c.1847C>A	XP_011517328.1:p.Ser616Ter
XM_011519027.1:c.1991C>A	XP_011517329.1:p.Ser664Ter
XM_011519028.1:c.1991C>A	XP_011517330.1:p.Ser664Ter
XM_011519029.1:c.413C>A	XP_011517331.1:p.Ser138Ter
XM_011519033.1:c.1826C>A	XP_011517335.1:p.Ser609Ter
NM_001354259.1:c.1889C>A	NP_001341188.1:p.Ser630Ter
NM_001354263.1:c.1961C>A	NP_001341192.1:p.Ser654Ter
XM_005266105.5:c.1973C>A	XP_005266162.1:p.Ser658Ter
XM_011519021.3:c.1991C>A	XP_011517323.1:p.Ser664Ter
XM_011519022.3:c.1988C>A	XP_011517324.1:p.Ser663Ter
XM_011519023.3:c.1970C>A	XP_011517325.1:p.Ser657Ter
XM_011519029.3:c.413C>A	XP_011517331.1:p.Ser138Ter
XM_017015134.1:c.1967C>A	XP_016870623.1:p.Ser656Ter
XM_017015136.2:c.1883C>A	XP_016870625.1:p.Ser628Ter
XM_017015137.1:c.1868C>A	XP_016870626.1:p.Ser623Ter
XM_017015138.1:c.1868C>A	XP_016870627.1:p.Ser623Ter
XM_024447674.1:c.1811C>A	XP_024303442.1:p.Ser604Ter
XM_024447675.1:c.1745C>A	XP_024303443.1:p.Ser582Ter
XM_024447676.1:c.1106C>A	XP_024303444.1:p.Ser369Ter
XM_024447677.1:c.1106C>A	XP_024303445.1:p.Ser369Ter
XM_024447678.1:c.1889C>A	XP_024303446.1:p.Ser630Ter
XM_024447679.1:c.1889C>A	XP_024303447.1:p.Ser630Ter
XM_024447680.1:c.1724C>A	XP_024303448.1:p.Ser575Ter
NM_024757.5:c.1982C>A MANE Select	NP_079033.4:p.Ser661Ter
NM_001145527.2:c.1982C>A	NP_001138999.1:p.Ser661Ter
NM_001354259.2:c.1889C>A	NP_001341188.1:p.Ser630Ter
NM_001354263.2:c.1961C>A	NP_001341192.1:p.Ser654Ter