Canonical Allele Identifier: CA375776883

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671257G>T (hg19) ; chr9:g.137776805G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776805G>T , CM000671.2:g.137776805G>T	GRCh38
NC_000009.11:g.140671257G>T , CM000671.1:g.140671257G>T	GRCh37
NC_000009.10:g.139791078G>T	NCBI36
NG_011776.1:g.162814G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1979G>T MANE Select	ENSP00000417980.1:p.Gly660Val
ENST00000636027.1:c.1865G>T	ENSP00000489961.1:p.Gly622Val
ENST00000637161.1:c.1886G>T	ENSP00000490328.1:p.Gly629Val
ENST00000637261.1:c.2019G>T	ENSP00000490815.1:n.2019G>T
ENST00000638071.1:c.1606G>T
ENST00000640639.1:c.1148G>T	ENSP00000491823.1:p.Gly383Val
ENST00000371394.6:c.*1714G>T	ENSP00000485945.1:n.*1714G>T
ENST00000460843.5:c.1979G>T	ENSP00000417980.1:p.Gly660Val
ENST00000462484.5:c.1979G>T	ENSP00000417328.1:p.Gly660Val
ENST00000462942.3:c.836G>T	ENSP00000436107.1:p.Gly279Val
ENST00000626603.1:n.1644C>A
NM_001145527.1:c.1979G>T	NP_001138999.1:p.Gly660Val
NM_024757.4:c.1979G>T	NP_079033.4:p.Gly660Val
XM_005266105.3:c.1970G>T	XP_005266162.1:p.Gly657Val
XM_005266110.1:c.1886G>T	XP_005266167.1:p.Gly629Val
XM_006717288.2:c.1961G>T	XP_006717351.1:p.Gly654Val
XM_011519021.1:c.1988G>T	XP_011517323.1:p.Gly663Val
XM_011519022.1:c.1985G>T	XP_011517324.1:p.Gly662Val
XM_011519023.1:c.1967G>T	XP_011517325.1:p.Gly656Val
XM_011519024.1:c.1910G>T	XP_011517326.1:p.Gly637Val
XM_011519025.1:c.1886G>T	XP_011517327.1:p.Gly629Val
XM_011519026.1:c.1844G>T	XP_011517328.1:p.Gly615Val
XM_011519027.1:c.1988G>T	XP_011517329.1:p.Gly663Val
XM_011519028.1:c.1988G>T	XP_011517330.1:p.Gly663Val
XM_011519029.1:c.410G>T	XP_011517331.1:p.Gly137Val
XM_011519033.1:c.1823G>T	XP_011517335.1:p.Gly608Val
NM_001354259.1:c.1886G>T	NP_001341188.1:p.Gly629Val
NM_001354263.1:c.1958G>T	NP_001341192.1:p.Gly653Val
XM_005266105.5:c.1970G>T	XP_005266162.1:p.Gly657Val
XM_011519021.3:c.1988G>T	XP_011517323.1:p.Gly663Val
XM_011519022.3:c.1985G>T	XP_011517324.1:p.Gly662Val
XM_011519023.3:c.1967G>T	XP_011517325.1:p.Gly656Val
XM_011519029.3:c.410G>T	XP_011517331.1:p.Gly137Val
XM_017015134.1:c.1964G>T	XP_016870623.1:p.Gly655Val
XM_017015136.2:c.1880G>T	XP_016870625.1:p.Gly627Val
XM_017015137.1:c.1865G>T	XP_016870626.1:p.Gly622Val
XM_017015138.1:c.1865G>T	XP_016870627.1:p.Gly622Val
XM_024447674.1:c.1808G>T	XP_024303442.1:p.Gly603Val
XM_024447675.1:c.1742G>T	XP_024303443.1:p.Gly581Val
XM_024447676.1:c.1103G>T	XP_024303444.1:p.Gly368Val
XM_024447677.1:c.1103G>T	XP_024303445.1:p.Gly368Val
XM_024447678.1:c.1886G>T	XP_024303446.1:p.Gly629Val
XM_024447679.1:c.1886G>T	XP_024303447.1:p.Gly629Val
XM_024447680.1:c.1721G>T	XP_024303448.1:p.Gly574Val
NM_024757.5:c.1979G>T MANE Select	NP_079033.4:p.Gly660Val
NM_001145527.2:c.1979G>T	NP_001138999.1:p.Gly660Val
NM_001354259.2:c.1886G>T	NP_001341188.1:p.Gly629Val
NM_001354263.2:c.1958G>T	NP_001341192.1:p.Gly653Val