Canonical Allele Identifier: CA375776743

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671232A>T (hg19) ; chr9:g.137776780A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776780A>T , CM000671.2:g.137776780A>T	GRCh38
NC_000009.11:g.140671232A>T , CM000671.1:g.140671232A>T	GRCh37
NC_000009.10:g.139791053A>T	NCBI36
NG_011776.1:g.162789A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1954A>T MANE Select	ENSP00000417980.1:p.Thr652Ser
ENST00000636027.1:c.1840A>T	ENSP00000489961.1:p.Thr614Ser
ENST00000637161.1:c.1861A>T	ENSP00000490328.1:p.Thr621Ser
ENST00000637261.1:c.1994A>T	ENSP00000490815.1:n.1994A>T
ENST00000638071.1:c.1581A>T
ENST00000640639.1:c.1123A>T	ENSP00000491823.1:p.Thr375Ser
ENST00000371394.6:c.*1689A>T	ENSP00000485945.1:n.*1689A>T
ENST00000460843.5:c.1954A>T	ENSP00000417980.1:p.Thr652Ser
ENST00000462484.5:c.1954A>T	ENSP00000417328.1:p.Thr652Ser
ENST00000462942.3:c.811A>T	ENSP00000436107.1:p.Thr271Ser
ENST00000465566.2:c.502A>T
ENST00000626603.1:n.1669T>A
NM_001145527.1:c.1954A>T	NP_001138999.1:p.Thr652Ser
NM_024757.4:c.1954A>T	NP_079033.4:p.Thr652Ser
XM_005266105.3:c.1945A>T	XP_005266162.1:p.Thr649Ser
XM_005266110.1:c.1861A>T	XP_005266167.1:p.Thr621Ser
XM_006717288.2:c.1936A>T	XP_006717351.1:p.Thr646Ser
XM_011519021.1:c.1963A>T	XP_011517323.1:p.Thr655Ser
XM_011519022.1:c.1960A>T	XP_011517324.1:p.Thr654Ser
XM_011519023.1:c.1942A>T	XP_011517325.1:p.Thr648Ser
XM_011519024.1:c.1885A>T	XP_011517326.1:p.Thr629Ser
XM_011519025.1:c.1861A>T	XP_011517327.1:p.Thr621Ser
XM_011519026.1:c.1819A>T	XP_011517328.1:p.Thr607Ser
XM_011519027.1:c.1963A>T	XP_011517329.1:p.Thr655Ser
XM_011519028.1:c.1963A>T	XP_011517330.1:p.Thr655Ser
XM_011519029.1:c.385A>T	XP_011517331.1:p.Thr129Ser
XM_011519033.1:c.1798A>T	XP_011517335.1:p.Thr600Ser
NM_001354259.1:c.1861A>T	NP_001341188.1:p.Thr621Ser
NM_001354263.1:c.1933A>T	NP_001341192.1:p.Thr645Ser
XM_005266105.5:c.1945A>T	XP_005266162.1:p.Thr649Ser
XM_011519021.3:c.1963A>T	XP_011517323.1:p.Thr655Ser
XM_011519022.3:c.1960A>T	XP_011517324.1:p.Thr654Ser
XM_011519023.3:c.1942A>T	XP_011517325.1:p.Thr648Ser
XM_011519029.3:c.385A>T	XP_011517331.1:p.Thr129Ser
XM_017015134.1:c.1939A>T	XP_016870623.1:p.Thr647Ser
XM_017015136.2:c.1855A>T	XP_016870625.1:p.Thr619Ser
XM_017015137.1:c.1840A>T	XP_016870626.1:p.Thr614Ser
XM_017015138.1:c.1840A>T	XP_016870627.1:p.Thr614Ser
XM_024447674.1:c.1783A>T	XP_024303442.1:p.Thr595Ser
XM_024447675.1:c.1717A>T	XP_024303443.1:p.Thr573Ser
XM_024447676.1:c.1078A>T	XP_024303444.1:p.Thr360Ser
XM_024447677.1:c.1078A>T	XP_024303445.1:p.Thr360Ser
XM_024447678.1:c.1861A>T	XP_024303446.1:p.Thr621Ser
XM_024447679.1:c.1861A>T	XP_024303447.1:p.Thr621Ser
XM_024447680.1:c.1696A>T	XP_024303448.1:p.Thr566Ser
NM_024757.5:c.1954A>T MANE Select	NP_079033.4:p.Thr652Ser
NM_001145527.2:c.1954A>T	NP_001138999.1:p.Thr652Ser
NM_001354259.2:c.1861A>T	NP_001341188.1:p.Thr621Ser
NM_001354263.2:c.1933A>T	NP_001341192.1:p.Thr645Ser