Canonical Allele Identifier: CA375776971

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671274A>T (hg19) ; chr9:g.137776822A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776822A>T , CM000671.2:g.137776822A>T	GRCh38
NC_000009.11:g.140671274A>T , CM000671.1:g.140671274A>T	GRCh37
NC_000009.10:g.139791095A>T	NCBI36
NG_011776.1:g.162831A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1996A>T MANE Select	ENSP00000417980.1:p.Arg666Trp
ENST00000636027.1:c.1882A>T	ENSP00000489961.1:p.Arg628Trp
ENST00000637161.1:c.1903A>T	ENSP00000490328.1:p.Arg635Trp
ENST00000637261.1:c.2036A>T	ENSP00000490815.1:n.2036A>T
ENST00000638071.1:c.1623A>T
ENST00000640639.1:c.1165A>T	ENSP00000491823.1:p.Arg389Trp
ENST00000371394.6:c.*1731A>T	ENSP00000485945.1:n.*1731A>T
ENST00000460843.5:c.1996A>T	ENSP00000417980.1:p.Arg666Trp
ENST00000462484.5:c.1996A>T	ENSP00000417328.1:p.Arg666Trp
ENST00000462942.3:c.853A>T	ENSP00000436107.1:p.Arg285Trp
ENST00000626603.1:n.1627T>A
NM_001145527.1:c.1996A>T	NP_001138999.1:p.Arg666Trp
NM_024757.4:c.1996A>T	NP_079033.4:p.Arg666Trp
XM_005266105.3:c.1987A>T	XP_005266162.1:p.Arg663Trp
XM_005266110.1:c.1903A>T	XP_005266167.1:p.Arg635Trp
XM_006717288.2:c.1978A>T	XP_006717351.1:p.Arg660Trp
XM_011519021.1:c.2005A>T	XP_011517323.1:p.Arg669Trp
XM_011519022.1:c.2002A>T	XP_011517324.1:p.Arg668Trp
XM_011519023.1:c.1984A>T	XP_011517325.1:p.Arg662Trp
XM_011519024.1:c.1927A>T	XP_011517326.1:p.Arg643Trp
XM_011519025.1:c.1903A>T	XP_011517327.1:p.Arg635Trp
XM_011519026.1:c.1861A>T	XP_011517328.1:p.Arg621Trp
XM_011519027.1:c.2005A>T	XP_011517329.1:p.Arg669Trp
XM_011519028.1:c.2005A>T	XP_011517330.1:p.Arg669Trp
XM_011519029.1:c.427A>T	XP_011517331.1:p.Arg143Trp
XM_011519033.1:c.1840A>T	XP_011517335.1:p.Arg614Trp
NM_001354259.1:c.1903A>T	NP_001341188.1:p.Arg635Trp
NM_001354263.1:c.1975A>T	NP_001341192.1:p.Arg659Trp
XM_005266105.5:c.1987A>T	XP_005266162.1:p.Arg663Trp
XM_011519021.3:c.2005A>T	XP_011517323.1:p.Arg669Trp
XM_011519022.3:c.2002A>T	XP_011517324.1:p.Arg668Trp
XM_011519023.3:c.1984A>T	XP_011517325.1:p.Arg662Trp
XM_011519029.3:c.427A>T	XP_011517331.1:p.Arg143Trp
XM_017015134.1:c.1981A>T	XP_016870623.1:p.Arg661Trp
XM_017015136.2:c.1897A>T	XP_016870625.1:p.Arg633Trp
XM_017015137.1:c.1882A>T	XP_016870626.1:p.Arg628Trp
XM_017015138.1:c.1882A>T	XP_016870627.1:p.Arg628Trp
XM_024447674.1:c.1825A>T	XP_024303442.1:p.Arg609Trp
XM_024447675.1:c.1759A>T	XP_024303443.1:p.Arg587Trp
XM_024447676.1:c.1120A>T	XP_024303444.1:p.Arg374Trp
XM_024447677.1:c.1120A>T	XP_024303445.1:p.Arg374Trp
XM_024447678.1:c.1903A>T	XP_024303446.1:p.Arg635Trp
XM_024447679.1:c.1903A>T	XP_024303447.1:p.Arg635Trp
XM_024447680.1:c.1738A>T	XP_024303448.1:p.Arg580Trp
NM_024757.5:c.1996A>T MANE Select	NP_079033.4:p.Arg666Trp
NM_001145527.2:c.1996A>T	NP_001138999.1:p.Arg666Trp
NM_001354259.2:c.1903A>T	NP_001341188.1:p.Arg635Trp
NM_001354263.2:c.1975A>T	NP_001341192.1:p.Arg659Trp