Canonical Allele Identifier: CA375777013

Gene: EHMT1

Linked Data

• gnomAD v4: 9-137776829-A-T
• MyVariant Identifiers: chr9:g.140671281A>T (hg19) ; chr9:g.137776829A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776829A>T , CM000671.2:g.137776829A>T	GRCh38
NC_000009.11:g.140671281A>T , CM000671.1:g.140671281A>T	GRCh37
NC_000009.10:g.139791102A>T	NCBI36
NG_011776.1:g.162838A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2003A>T MANE Select	ENSP00000417980.1:p.Asp668Val
ENST00000636027.1:c.1889A>T	ENSP00000489961.1:p.Asp630Val
ENST00000637161.1:c.1910A>T	ENSP00000490328.1:p.Asp637Val
ENST00000637261.1:c.2043A>T	ENSP00000490815.1:n.2043A>T
ENST00000638071.1:c.1630A>T
ENST00000640639.1:c.1172A>T	ENSP00000491823.1:p.Asp391Val
ENST00000371394.6:c.*1738A>T	ENSP00000485945.1:n.*1738A>T
ENST00000460843.5:c.2003A>T	ENSP00000417980.1:p.Asp668Val
ENST00000462484.5:c.2003A>T	ENSP00000417328.1:p.Asp668Val
ENST00000462942.3:c.860A>T	ENSP00000436107.1:p.Asp287Val
ENST00000626603.1:n.1620T>A
NM_001145527.1:c.2003A>T	NP_001138999.1:p.Asp668Val
NM_024757.4:c.2003A>T	NP_079033.4:p.Asp668Val
XM_005266105.3:c.1994A>T	XP_005266162.1:p.Asp665Val
XM_005266110.1:c.1910A>T	XP_005266167.1:p.Asp637Val
XM_006717288.2:c.1985A>T	XP_006717351.1:p.Asp662Val
XM_011519021.1:c.2012A>T	XP_011517323.1:p.Asp671Val
XM_011519022.1:c.2009A>T	XP_011517324.1:p.Asp670Val
XM_011519023.1:c.1991A>T	XP_011517325.1:p.Asp664Val
XM_011519024.1:c.1934A>T	XP_011517326.1:p.Asp645Val
XM_011519025.1:c.1910A>T	XP_011517327.1:p.Asp637Val
XM_011519026.1:c.1868A>T	XP_011517328.1:p.Asp623Val
XM_011519027.1:c.2012A>T	XP_011517329.1:p.Asp671Val
XM_011519028.1:c.2012A>T	XP_011517330.1:p.Asp671Val
XM_011519029.1:c.434A>T	XP_011517331.1:p.Asp145Val
XM_011519033.1:c.1847A>T	XP_011517335.1:p.Asp616Val
NM_001354259.1:c.1910A>T	NP_001341188.1:p.Asp637Val
NM_001354263.1:c.1982A>T	NP_001341192.1:p.Asp661Val
XM_005266105.5:c.1994A>T	XP_005266162.1:p.Asp665Val
XM_011519021.3:c.2012A>T	XP_011517323.1:p.Asp671Val
XM_011519022.3:c.2009A>T	XP_011517324.1:p.Asp670Val
XM_011519023.3:c.1991A>T	XP_011517325.1:p.Asp664Val
XM_011519029.3:c.434A>T	XP_011517331.1:p.Asp145Val
XM_017015134.1:c.1988A>T	XP_016870623.1:p.Asp663Val
XM_017015136.2:c.1904A>T	XP_016870625.1:p.Asp635Val
XM_017015137.1:c.1889A>T	XP_016870626.1:p.Asp630Val
XM_017015138.1:c.1889A>T	XP_016870627.1:p.Asp630Val
XM_024447674.1:c.1832A>T	XP_024303442.1:p.Asp611Val
XM_024447675.1:c.1766A>T	XP_024303443.1:p.Asp589Val
XM_024447676.1:c.1127A>T	XP_024303444.1:p.Asp376Val
XM_024447677.1:c.1127A>T	XP_024303445.1:p.Asp376Val
XM_024447678.1:c.1910A>T	XP_024303446.1:p.Asp637Val
XM_024447679.1:c.1910A>T	XP_024303447.1:p.Asp637Val
XM_024447680.1:c.1745A>T	XP_024303448.1:p.Asp582Val
NM_024757.5:c.2003A>T MANE Select	NP_079033.4:p.Asp668Val
NM_001145527.2:c.2003A>T	NP_001138999.1:p.Asp668Val
NM_001354259.2:c.1910A>T	NP_001341188.1:p.Asp637Val
NM_001354263.2:c.1982A>T	NP_001341192.1:p.Asp661Val