Canonical Allele Identifier: CA375776395

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671188C>A (hg19) ; chr9:g.137776736C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776736C>A , CM000671.2:g.137776736C>A	GRCh38
NC_000009.11:g.140671188C>A , CM000671.1:g.140671188C>A	GRCh37
NC_000009.10:g.139791009C>A	NCBI36
NG_011776.1:g.162745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1910C>A MANE Select	ENSP00000417980.1:p.Ala637Asp
ENST00000636027.1:c.1796C>A	ENSP00000489961.1:p.Ala599Asp
ENST00000637161.1:c.1817C>A	ENSP00000490328.1:p.Ala606Asp
ENST00000637261.1:c.1950C>A	ENSP00000490815.1:n.1950C>A
ENST00000638071.1:c.1537C>A
ENST00000640639.1:c.1079C>A	ENSP00000491823.1:p.Ala360Asp
ENST00000371394.6:c.*1645C>A	ENSP00000485945.1:n.*1645C>A
ENST00000460843.5:c.1910C>A	ENSP00000417980.1:p.Ala637Asp
ENST00000462484.5:c.1910C>A	ENSP00000417328.1:p.Ala637Asp
ENST00000462942.3:c.767C>A	ENSP00000436107.1:p.Ala256Asp
ENST00000465566.2:c.458C>A	ENSP00000486261.1:p.Ala153Asp
ENST00000626603.1:n.1713G>T
NM_001145527.1:c.1910C>A	NP_001138999.1:p.Ala637Asp
NM_024757.4:c.1910C>A	NP_079033.4:p.Ala637Asp
XM_005266105.3:c.1901C>A	XP_005266162.1:p.Ala634Asp
XM_005266110.1:c.1817C>A	XP_005266167.1:p.Ala606Asp
XM_006717288.2:c.1892C>A	XP_006717351.1:p.Ala631Asp
XM_011519021.1:c.1919C>A	XP_011517323.1:p.Ala640Asp
XM_011519022.1:c.1916C>A	XP_011517324.1:p.Ala639Asp
XM_011519023.1:c.1898C>A	XP_011517325.1:p.Ala633Asp
XM_011519024.1:c.1841C>A	XP_011517326.1:p.Ala614Asp
XM_011519025.1:c.1817C>A	XP_011517327.1:p.Ala606Asp
XM_011519026.1:c.1775C>A	XP_011517328.1:p.Ala592Asp
XM_011519027.1:c.1919C>A	XP_011517329.1:p.Ala640Asp
XM_011519028.1:c.1919C>A	XP_011517330.1:p.Ala640Asp
XM_011519029.1:c.341C>A	XP_011517331.1:p.Ala114Asp
XM_011519033.1:c.1754C>A	XP_011517335.1:p.Ala585Asp
NM_001354259.1:c.1817C>A	NP_001341188.1:p.Ala606Asp
NM_001354263.1:c.1889C>A	NP_001341192.1:p.Ala630Asp
XM_005266105.5:c.1901C>A	XP_005266162.1:p.Ala634Asp
XM_011519021.3:c.1919C>A	XP_011517323.1:p.Ala640Asp
XM_011519022.3:c.1916C>A	XP_011517324.1:p.Ala639Asp
XM_011519023.3:c.1898C>A	XP_011517325.1:p.Ala633Asp
XM_011519029.3:c.341C>A	XP_011517331.1:p.Ala114Asp
XM_017015134.1:c.1895C>A	XP_016870623.1:p.Ala632Asp
XM_017015136.2:c.1811C>A	XP_016870625.1:p.Ala604Asp
XM_017015137.1:c.1796C>A	XP_016870626.1:p.Ala599Asp
XM_017015138.1:c.1796C>A	XP_016870627.1:p.Ala599Asp
XM_024447674.1:c.1739C>A	XP_024303442.1:p.Ala580Asp
XM_024447675.1:c.1673C>A	XP_024303443.1:p.Ala558Asp
XM_024447676.1:c.1034C>A	XP_024303444.1:p.Ala345Asp
XM_024447677.1:c.1034C>A	XP_024303445.1:p.Ala345Asp
XM_024447678.1:c.1817C>A	XP_024303446.1:p.Ala606Asp
XM_024447679.1:c.1817C>A	XP_024303447.1:p.Ala606Asp
XM_024447680.1:c.1652C>A	XP_024303448.1:p.Ala551Asp
NM_024757.5:c.1910C>A MANE Select	NP_079033.4:p.Ala637Asp
NM_001145527.2:c.1910C>A	NP_001138999.1:p.Ala637Asp
NM_001354259.2:c.1817C>A	NP_001341188.1:p.Ala606Asp
NM_001354263.2:c.1889C>A	NP_001341192.1:p.Ala630Asp