Canonical Allele Identifier: CA375788786

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695357T>G (hg19) ; chr9:g.137800905T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800905T>G , CM000671.2:g.137800905T>G	GRCh38
NC_000009.11:g.140695357T>G , CM000671.1:g.140695357T>G	GRCh37
NC_000009.10:g.139815178T>G	NCBI36
NG_011776.1:g.186914T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2633T>G MANE Select	ENSP00000417980.1:p.Ile878Ser
ENST00000636027.1:c.2519T>G	ENSP00000489961.1:p.Ile840Ser
ENST00000637161.1:c.2540T>G	ENSP00000490328.1:p.Ile847Ser
ENST00000637261.1:c.2673T>G	ENSP00000490815.1:n.2673T>G
ENST00000637891.1:c.527T>G	ENSP00000490907.1:p.Ile176Ser
ENST00000637949.1:c.311T>G	ENSP00000489786.1:p.Ile104Ser
ENST00000460843.5:c.2633T>G	ENSP00000417980.1:p.Ile878Ser
ENST00000462942.3:c.1490T>G	ENSP00000436107.1:p.Ile497Ser
ENST00000482340.5:c.203T>G	ENSP00000486748.1:p.Ile68Ser
ENST00000486164.5:c.211T>G
ENST00000488242.2:n.159T>G
ENST00000493484.5:c.203T>G	ENSP00000486503.1:p.Ile68Ser
NM_024757.4:c.2633T>G	NP_079033.4:p.Ile878Ser
XM_005266105.3:c.2624T>G	XP_005266162.1:p.Ile875Ser
XM_005266110.1:c.2540T>G	XP_005266167.1:p.Ile847Ser
XM_006717288.2:c.2615T>G	XP_006717351.1:p.Ile872Ser
XM_011519021.1:c.2642T>G	XP_011517323.1:p.Ile881Ser
XM_011519022.1:c.2639T>G	XP_011517324.1:p.Ile880Ser
XM_011519023.1:c.2621T>G	XP_011517325.1:p.Ile874Ser
XM_011519024.1:c.2564T>G	XP_011517326.1:p.Ile855Ser
XM_011519025.1:c.2540T>G	XP_011517327.1:p.Ile847Ser
XM_011519026.1:c.2498T>G	XP_011517328.1:p.Ile833Ser
XM_011519027.1:c.2642T>G	XP_011517329.1:p.Ile881Ser
XM_011519029.1:c.1064T>G	XP_011517331.1:p.Ile355Ser
XM_011519030.1:c.416T>G	XP_011517332.1:p.Ile139Ser
XM_011519031.1:c.203T>G	XP_011517333.1:p.Ile68Ser
XM_011519032.1:c.203T>G	XP_011517334.1:p.Ile68Ser
XM_011519033.1:c.2477T>G	XP_011517335.1:p.Ile826Ser
NM_001354263.1:c.2612T>G	NP_001341192.1:p.Ile871Ser
XM_005266105.5:c.2624T>G	XP_005266162.1:p.Ile875Ser
XM_011519021.3:c.2642T>G	XP_011517323.1:p.Ile881Ser
XM_011519022.3:c.2639T>G	XP_011517324.1:p.Ile880Ser
XM_011519023.3:c.2621T>G	XP_011517325.1:p.Ile874Ser
XM_011519029.3:c.1064T>G	XP_011517331.1:p.Ile355Ser
XM_011519030.3:c.416T>G	XP_011517332.1:p.Ile139Ser
XM_017015134.1:c.2618T>G	XP_016870623.1:p.Ile873Ser
XM_017015136.2:c.2534T>G	XP_016870625.1:p.Ile845Ser
XM_017015137.1:c.2519T>G	XP_016870626.1:p.Ile840Ser
XM_017015138.1:c.2519T>G	XP_016870627.1:p.Ile840Ser
XM_024447674.1:c.2462T>G	XP_024303442.1:p.Ile821Ser
XM_024447675.1:c.2396T>G	XP_024303443.1:p.Ile799Ser
XM_024447676.1:c.1757T>G	XP_024303444.1:p.Ile586Ser
XM_024447677.1:c.1757T>G	XP_024303445.1:p.Ile586Ser
XM_024447678.1:c.2540T>G	XP_024303446.1:p.Ile847Ser
XM_024447680.1:c.2375T>G	XP_024303448.1:p.Ile792Ser
NM_024757.5:c.2633T>G MANE Select	NP_079033.4:p.Ile878Ser
NM_001354263.2:c.2612T>G	NP_001341192.1:p.Ile871Ser