Canonical Allele Identifier: CA375777032

Gene: EHMT1

Linked Data

• dbSNP Id: rs2136686639
• MyVariant Identifiers: chr9:g.140671284C>G (hg19) ; chr9:g.137776832C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776832C>G , CM000671.2:g.137776832C>G	GRCh38
NC_000009.11:g.140671284C>G , CM000671.1:g.140671284C>G	GRCh37
NC_000009.10:g.139791105C>G	NCBI36
NG_011776.1:g.162841C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2006C>G MANE Select	ENSP00000417980.1:p.Thr669Ser
ENST00000636027.1:c.1892C>G	ENSP00000489961.1:p.Thr631Ser
ENST00000637161.1:c.1913C>G	ENSP00000490328.1:p.Thr638Ser
ENST00000637261.1:c.2046C>G	ENSP00000490815.1:n.2046C>G
ENST00000638071.1:c.1633C>G
ENST00000640639.1:c.1175C>G	ENSP00000491823.1:p.Thr392Ser
ENST00000371394.6:c.*1741C>G	ENSP00000485945.1:n.*1741C>G
ENST00000460843.5:c.2006C>G	ENSP00000417980.1:p.Thr669Ser
ENST00000462484.5:c.2006C>G	ENSP00000417328.1:p.Thr669Ser
ENST00000462942.3:c.863C>G	ENSP00000436107.1:p.Thr288Ser
ENST00000626603.1:n.1617G>C
NM_001145527.1:c.2006C>G	NP_001138999.1:p.Thr669Ser
NM_024757.4:c.2006C>G	NP_079033.4:p.Thr669Ser
XM_005266105.3:c.1997C>G	XP_005266162.1:p.Thr666Ser
XM_005266110.1:c.1913C>G	XP_005266167.1:p.Thr638Ser
XM_006717288.2:c.1988C>G	XP_006717351.1:p.Thr663Ser
XM_011519021.1:c.2015C>G	XP_011517323.1:p.Thr672Ser
XM_011519022.1:c.2012C>G	XP_011517324.1:p.Thr671Ser
XM_011519023.1:c.1994C>G	XP_011517325.1:p.Thr665Ser
XM_011519024.1:c.1937C>G	XP_011517326.1:p.Thr646Ser
XM_011519025.1:c.1913C>G	XP_011517327.1:p.Thr638Ser
XM_011519026.1:c.1871C>G	XP_011517328.1:p.Thr624Ser
XM_011519027.1:c.2015C>G	XP_011517329.1:p.Thr672Ser
XM_011519028.1:c.2015C>G	XP_011517330.1:p.Thr672Ser
XM_011519029.1:c.437C>G	XP_011517331.1:p.Thr146Ser
XM_011519033.1:c.1850C>G	XP_011517335.1:p.Thr617Ser
NM_001354259.1:c.1913C>G	NP_001341188.1:p.Thr638Ser
NM_001354263.1:c.1985C>G	NP_001341192.1:p.Thr662Ser
XM_005266105.5:c.1997C>G	XP_005266162.1:p.Thr666Ser
XM_011519021.3:c.2015C>G	XP_011517323.1:p.Thr672Ser
XM_011519022.3:c.2012C>G	XP_011517324.1:p.Thr671Ser
XM_011519023.3:c.1994C>G	XP_011517325.1:p.Thr665Ser
XM_011519029.3:c.437C>G	XP_011517331.1:p.Thr146Ser
XM_017015134.1:c.1991C>G	XP_016870623.1:p.Thr664Ser
XM_017015136.2:c.1907C>G	XP_016870625.1:p.Thr636Ser
XM_017015137.1:c.1892C>G	XP_016870626.1:p.Thr631Ser
XM_017015138.1:c.1892C>G	XP_016870627.1:p.Thr631Ser
XM_024447674.1:c.1835C>G	XP_024303442.1:p.Thr612Ser
XM_024447675.1:c.1769C>G	XP_024303443.1:p.Thr590Ser
XM_024447676.1:c.1130C>G	XP_024303444.1:p.Thr377Ser
XM_024447677.1:c.1130C>G	XP_024303445.1:p.Thr377Ser
XM_024447678.1:c.1913C>G	XP_024303446.1:p.Thr638Ser
XM_024447679.1:c.1913C>G	XP_024303447.1:p.Thr638Ser
XM_024447680.1:c.1748C>G	XP_024303448.1:p.Thr583Ser
NM_024757.5:c.2006C>G MANE Select	NP_079033.4:p.Thr669Ser
NM_001145527.2:c.2006C>G	NP_001138999.1:p.Thr669Ser
NM_001354259.2:c.1913C>G	NP_001341188.1:p.Thr638Ser
NM_001354263.2:c.1985C>G	NP_001341192.1:p.Thr662Ser