Canonical Allele Identifier: CA375777076

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671296G>C (hg19) ; chr9:g.137776844G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776844G>C , CM000671.2:g.137776844G>C	GRCh38
NC_000009.11:g.140671296G>C , CM000671.1:g.140671296G>C	GRCh37
NC_000009.10:g.139791117G>C	NCBI36
NG_011776.1:g.162853G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2018G>C MANE Select	ENSP00000417980.1:p.Ser673Thr
ENST00000636027.1:c.1904G>C	ENSP00000489961.1:p.Ser635Thr
ENST00000637161.1:c.1925G>C	ENSP00000490328.1:p.Ser642Thr
ENST00000637261.1:c.2058G>C	ENSP00000490815.1:n.2058G>C
ENST00000638071.1:c.1645G>C
ENST00000371394.6:c.*1753G>C	ENSP00000485945.1:n.*1753G>C
ENST00000460843.5:c.2018G>C	ENSP00000417980.1:p.Ser673Thr
ENST00000462484.5:c.2018G>C	ENSP00000417328.1:p.Ser673Thr
ENST00000462942.3:c.875G>C	ENSP00000436107.1:p.Ser292Thr
ENST00000626603.1:n.1605C>G
NM_001145527.1:c.2018G>C	NP_001138999.1:p.Ser673Thr
NM_024757.4:c.2018G>C	NP_079033.4:p.Ser673Thr
XM_005266105.3:c.2009G>C	XP_005266162.1:p.Ser670Thr
XM_005266110.1:c.1925G>C	XP_005266167.1:p.Ser642Thr
XM_006717288.2:c.2000G>C	XP_006717351.1:p.Ser667Thr
XM_011519021.1:c.2027G>C	XP_011517323.1:p.Ser676Thr
XM_011519022.1:c.2024G>C	XP_011517324.1:p.Ser675Thr
XM_011519023.1:c.2006G>C	XP_011517325.1:p.Ser669Thr
XM_011519024.1:c.1949G>C	XP_011517326.1:p.Ser650Thr
XM_011519025.1:c.1925G>C	XP_011517327.1:p.Ser642Thr
XM_011519026.1:c.1883G>C	XP_011517328.1:p.Ser628Thr
XM_011519027.1:c.2027G>C	XP_011517329.1:p.Ser676Thr
XM_011519028.1:c.2027G>C	XP_011517330.1:p.Ser676Thr
XM_011519029.1:c.449G>C	XP_011517331.1:p.Ser150Thr
XM_011519033.1:c.1862G>C	XP_011517335.1:p.Ser621Thr
NM_001354259.1:c.1925G>C	NP_001341188.1:p.Ser642Thr
NM_001354263.1:c.1997G>C	NP_001341192.1:p.Ser666Thr
XM_005266105.5:c.2009G>C	XP_005266162.1:p.Ser670Thr
XM_011519021.3:c.2027G>C	XP_011517323.1:p.Ser676Thr
XM_011519022.3:c.2024G>C	XP_011517324.1:p.Ser675Thr
XM_011519023.3:c.2006G>C	XP_011517325.1:p.Ser669Thr
XM_011519029.3:c.449G>C	XP_011517331.1:p.Ser150Thr
XM_017015134.1:c.2003G>C	XP_016870623.1:p.Ser668Thr
XM_017015136.2:c.1919G>C	XP_016870625.1:p.Ser640Thr
XM_017015137.1:c.1904G>C	XP_016870626.1:p.Ser635Thr
XM_017015138.1:c.1904G>C	XP_016870627.1:p.Ser635Thr
XM_024447674.1:c.1847G>C	XP_024303442.1:p.Ser616Thr
XM_024447675.1:c.1781G>C	XP_024303443.1:p.Ser594Thr
XM_024447676.1:c.1142G>C	XP_024303444.1:p.Ser381Thr
XM_024447677.1:c.1142G>C	XP_024303445.1:p.Ser381Thr
XM_024447678.1:c.1925G>C	XP_024303446.1:p.Ser642Thr
XM_024447679.1:c.1925G>C	XP_024303447.1:p.Ser642Thr
XM_024447680.1:c.1760G>C	XP_024303448.1:p.Ser587Thr
NM_024757.5:c.2018G>C MANE Select	NP_079033.4:p.Ser673Thr
NM_001145527.2:c.2018G>C	NP_001138999.1:p.Ser673Thr
NM_001354259.2:c.1925G>C	NP_001341188.1:p.Ser642Thr
NM_001354263.2:c.1997G>C	NP_001341192.1:p.Ser666Thr