Canonical Allele Identifier: CA375775642

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671092C>G (hg19) ; chr9:g.137776640C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776640C>G , CM000671.2:g.137776640C>G	GRCh38
NC_000009.11:g.140671092C>G , CM000671.1:g.140671092C>G	GRCh37
NC_000009.10:g.139790913C>G	NCBI36
NG_011776.1:g.162649C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.1814C>G MANE Select	ENSP00000417980.1:p.Pro605Arg
ENST00000636027.1:c.1700C>G	ENSP00000489961.1:p.Pro567Arg
ENST00000637161.1:c.1721C>G	ENSP00000490328.1:p.Pro574Arg
ENST00000637261.1:c.1854C>G	ENSP00000490815.1:n.1854C>G
ENST00000638071.1:c.1441C>G
ENST00000640639.1:c.983C>G	ENSP00000491823.1:p.Pro328Arg
ENST00000371394.6:c.*1549C>G	ENSP00000485945.1:n.*1549C>G
ENST00000460843.5:c.1814C>G	ENSP00000417980.1:p.Pro605Arg
ENST00000462484.5:c.1814C>G	ENSP00000417328.1:p.Pro605Arg
ENST00000462942.3:c.671C>G	ENSP00000436107.1:p.Pro224Arg
ENST00000465566.2:c.362C>G	ENSP00000486261.1:p.Pro121Arg
ENST00000626603.1:n.1809G>C
NM_001145527.1:c.1814C>G	NP_001138999.1:p.Pro605Arg
NM_024757.4:c.1814C>G	NP_079033.4:p.Pro605Arg
XM_005266105.3:c.1805C>G	XP_005266162.1:p.Pro602Arg
XM_005266110.1:c.1721C>G	XP_005266167.1:p.Pro574Arg
XM_006717288.2:c.1796C>G	XP_006717351.1:p.Pro599Arg
XM_011519021.1:c.1823C>G	XP_011517323.1:p.Pro608Arg
XM_011519022.1:c.1820C>G	XP_011517324.1:p.Pro607Arg
XM_011519023.1:c.1802C>G	XP_011517325.1:p.Pro601Arg
XM_011519024.1:c.1745C>G	XP_011517326.1:p.Pro582Arg
XM_011519025.1:c.1721C>G	XP_011517327.1:p.Pro574Arg
XM_011519026.1:c.1679C>G	XP_011517328.1:p.Pro560Arg
XM_011519027.1:c.1823C>G	XP_011517329.1:p.Pro608Arg
XM_011519028.1:c.1823C>G	XP_011517330.1:p.Pro608Arg
XM_011519029.1:c.245C>G	XP_011517331.1:p.Pro82Arg
XM_011519033.1:c.1658C>G	XP_011517335.1:p.Pro553Arg
NM_001354259.1:c.1721C>G	NP_001341188.1:p.Pro574Arg
NM_001354263.1:c.1793C>G	NP_001341192.1:p.Pro598Arg
XM_005266105.5:c.1805C>G	XP_005266162.1:p.Pro602Arg
XM_011519021.3:c.1823C>G	XP_011517323.1:p.Pro608Arg
XM_011519022.3:c.1820C>G	XP_011517324.1:p.Pro607Arg
XM_011519023.3:c.1802C>G	XP_011517325.1:p.Pro601Arg
XM_011519029.3:c.245C>G	XP_011517331.1:p.Pro82Arg
XM_017015134.1:c.1799C>G	XP_016870623.1:p.Pro600Arg
XM_017015136.2:c.1715C>G	XP_016870625.1:p.Pro572Arg
XM_017015137.1:c.1700C>G	XP_016870626.1:p.Pro567Arg
XM_017015138.1:c.1700C>G	XP_016870627.1:p.Pro567Arg
XM_024447674.1:c.1643C>G	XP_024303442.1:p.Pro548Arg
XM_024447675.1:c.1577C>G	XP_024303443.1:p.Pro526Arg
XM_024447676.1:c.938C>G	XP_024303444.1:p.Pro313Arg
XM_024447677.1:c.938C>G	XP_024303445.1:p.Pro313Arg
XM_024447678.1:c.1721C>G	XP_024303446.1:p.Pro574Arg
XM_024447679.1:c.1721C>G	XP_024303447.1:p.Pro574Arg
XM_024447680.1:c.1556C>G	XP_024303448.1:p.Pro519Arg
NM_024757.5:c.1814C>G MANE Select	NP_079033.4:p.Pro605Arg
NM_001145527.2:c.1814C>G	NP_001138999.1:p.Pro605Arg
NM_001354259.2:c.1721C>G	NP_001341188.1:p.Pro574Arg
NM_001354263.2:c.1793C>G	NP_001341192.1:p.Pro598Arg