Canonical Allele Identifier: CA375776884

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140671259T>A (hg19) ; chr9:g.137776807T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137776807T>A , CM000671.2:g.137776807T>A	GRCh38
NC_000009.11:g.140671259T>A , CM000671.1:g.140671259T>A	GRCh37
NC_000009.10:g.139791080T>A	NCBI36
NG_011776.1:g.162816T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.1981T>A MANE Select	ENSP00000417980.1:p.Ser661Thr
ENST00000636027.1:c.1867T>A	ENSP00000489961.1:p.Ser623Thr
ENST00000637161.1:c.1888T>A	ENSP00000490328.1:p.Ser630Thr
ENST00000637261.1:c.2021T>A	ENSP00000490815.1:n.2021T>A
ENST00000638071.1:c.1608T>A
ENST00000640639.1:c.1150T>A	ENSP00000491823.1:p.Ser384Thr
ENST00000371394.6:c.*1716T>A	ENSP00000485945.1:n.*1716T>A
ENST00000460843.5:c.1981T>A	ENSP00000417980.1:p.Ser661Thr
ENST00000462484.5:c.1981T>A	ENSP00000417328.1:p.Ser661Thr
ENST00000462942.3:c.838T>A	ENSP00000436107.1:p.Ser280Thr
ENST00000626603.1:n.1642A>T
NM_001145527.1:c.1981T>A	NP_001138999.1:p.Ser661Thr
NM_024757.4:c.1981T>A	NP_079033.4:p.Ser661Thr
XM_005266105.3:c.1972T>A	XP_005266162.1:p.Ser658Thr
XM_005266110.1:c.1888T>A	XP_005266167.1:p.Ser630Thr
XM_006717288.2:c.1963T>A	XP_006717351.1:p.Ser655Thr
XM_011519021.1:c.1990T>A	XP_011517323.1:p.Ser664Thr
XM_011519022.1:c.1987T>A	XP_011517324.1:p.Ser663Thr
XM_011519023.1:c.1969T>A	XP_011517325.1:p.Ser657Thr
XM_011519024.1:c.1912T>A	XP_011517326.1:p.Ser638Thr
XM_011519025.1:c.1888T>A	XP_011517327.1:p.Ser630Thr
XM_011519026.1:c.1846T>A	XP_011517328.1:p.Ser616Thr
XM_011519027.1:c.1990T>A	XP_011517329.1:p.Ser664Thr
XM_011519028.1:c.1990T>A	XP_011517330.1:p.Ser664Thr
XM_011519029.1:c.412T>A	XP_011517331.1:p.Ser138Thr
XM_011519033.1:c.1825T>A	XP_011517335.1:p.Ser609Thr
NM_001354259.1:c.1888T>A	NP_001341188.1:p.Ser630Thr
NM_001354263.1:c.1960T>A	NP_001341192.1:p.Ser654Thr
XM_005266105.5:c.1972T>A	XP_005266162.1:p.Ser658Thr
XM_011519021.3:c.1990T>A	XP_011517323.1:p.Ser664Thr
XM_011519022.3:c.1987T>A	XP_011517324.1:p.Ser663Thr
XM_011519023.3:c.1969T>A	XP_011517325.1:p.Ser657Thr
XM_011519029.3:c.412T>A	XP_011517331.1:p.Ser138Thr
XM_017015134.1:c.1966T>A	XP_016870623.1:p.Ser656Thr
XM_017015136.2:c.1882T>A	XP_016870625.1:p.Ser628Thr
XM_017015137.1:c.1867T>A	XP_016870626.1:p.Ser623Thr
XM_017015138.1:c.1867T>A	XP_016870627.1:p.Ser623Thr
XM_024447674.1:c.1810T>A	XP_024303442.1:p.Ser604Thr
XM_024447675.1:c.1744T>A	XP_024303443.1:p.Ser582Thr
XM_024447676.1:c.1105T>A	XP_024303444.1:p.Ser369Thr
XM_024447677.1:c.1105T>A	XP_024303445.1:p.Ser369Thr
XM_024447678.1:c.1888T>A	XP_024303446.1:p.Ser630Thr
XM_024447679.1:c.1888T>A	XP_024303447.1:p.Ser630Thr
XM_024447680.1:c.1723T>A	XP_024303448.1:p.Ser575Thr
NM_024757.5:c.1981T>A MANE Select	NP_079033.4:p.Ser661Thr
NM_001145527.2:c.1981T>A	NP_001138999.1:p.Ser661Thr
NM_001354259.2:c.1888T>A	NP_001341188.1:p.Ser630Thr
NM_001354263.2:c.1960T>A	NP_001341192.1:p.Ser654Thr