Canonical Allele Identifier: CA375776748

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671233C>G (hg19) ; chr9:g.137776781C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776781C>G , CM000671.2:g.137776781C>G	GRCh38
NC_000009.11:g.140671233C>G , CM000671.1:g.140671233C>G	GRCh37
NC_000009.10:g.139791054C>G	NCBI36
NG_011776.1:g.162790C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1955C>G MANE Select	ENSP00000417980.1:p.Thr652Arg
ENST00000636027.1:c.1841C>G	ENSP00000489961.1:p.Thr614Arg
ENST00000637161.1:c.1862C>G	ENSP00000490328.1:p.Thr621Arg
ENST00000637261.1:c.1995C>G	ENSP00000490815.1:n.1995C>G
ENST00000638071.1:c.1582C>G
ENST00000640639.1:c.1124C>G	ENSP00000491823.1:p.Thr375Arg
ENST00000371394.6:c.*1690C>G	ENSP00000485945.1:n.*1690C>G
ENST00000460843.5:c.1955C>G	ENSP00000417980.1:p.Thr652Arg
ENST00000462484.5:c.1955C>G	ENSP00000417328.1:p.Thr652Arg
ENST00000462942.3:c.812C>G	ENSP00000436107.1:p.Thr271Arg
ENST00000465566.2:c.503C>G
ENST00000626603.1:n.1668G>C
NM_001145527.1:c.1955C>G	NP_001138999.1:p.Thr652Arg
NM_024757.4:c.1955C>G	NP_079033.4:p.Thr652Arg
XM_005266105.3:c.1946C>G	XP_005266162.1:p.Thr649Arg
XM_005266110.1:c.1862C>G	XP_005266167.1:p.Thr621Arg
XM_006717288.2:c.1937C>G	XP_006717351.1:p.Thr646Arg
XM_011519021.1:c.1964C>G	XP_011517323.1:p.Thr655Arg
XM_011519022.1:c.1961C>G	XP_011517324.1:p.Thr654Arg
XM_011519023.1:c.1943C>G	XP_011517325.1:p.Thr648Arg
XM_011519024.1:c.1886C>G	XP_011517326.1:p.Thr629Arg
XM_011519025.1:c.1862C>G	XP_011517327.1:p.Thr621Arg
XM_011519026.1:c.1820C>G	XP_011517328.1:p.Thr607Arg
XM_011519027.1:c.1964C>G	XP_011517329.1:p.Thr655Arg
XM_011519028.1:c.1964C>G	XP_011517330.1:p.Thr655Arg
XM_011519029.1:c.386C>G	XP_011517331.1:p.Thr129Arg
XM_011519033.1:c.1799C>G	XP_011517335.1:p.Thr600Arg
NM_001354259.1:c.1862C>G	NP_001341188.1:p.Thr621Arg
NM_001354263.1:c.1934C>G	NP_001341192.1:p.Thr645Arg
XM_005266105.5:c.1946C>G	XP_005266162.1:p.Thr649Arg
XM_011519021.3:c.1964C>G	XP_011517323.1:p.Thr655Arg
XM_011519022.3:c.1961C>G	XP_011517324.1:p.Thr654Arg
XM_011519023.3:c.1943C>G	XP_011517325.1:p.Thr648Arg
XM_011519029.3:c.386C>G	XP_011517331.1:p.Thr129Arg
XM_017015134.1:c.1940C>G	XP_016870623.1:p.Thr647Arg
XM_017015136.2:c.1856C>G	XP_016870625.1:p.Thr619Arg
XM_017015137.1:c.1841C>G	XP_016870626.1:p.Thr614Arg
XM_017015138.1:c.1841C>G	XP_016870627.1:p.Thr614Arg
XM_024447674.1:c.1784C>G	XP_024303442.1:p.Thr595Arg
XM_024447675.1:c.1718C>G	XP_024303443.1:p.Thr573Arg
XM_024447676.1:c.1079C>G	XP_024303444.1:p.Thr360Arg
XM_024447677.1:c.1079C>G	XP_024303445.1:p.Thr360Arg
XM_024447678.1:c.1862C>G	XP_024303446.1:p.Thr621Arg
XM_024447679.1:c.1862C>G	XP_024303447.1:p.Thr621Arg
XM_024447680.1:c.1697C>G	XP_024303448.1:p.Thr566Arg
NM_024757.5:c.1955C>G MANE Select	NP_079033.4:p.Thr652Arg
NM_001145527.2:c.1955C>G	NP_001138999.1:p.Thr652Arg
NM_001354259.2:c.1862C>G	NP_001341188.1:p.Thr621Arg
NM_001354263.2:c.1934C>G	NP_001341192.1:p.Thr645Arg