Canonical Allele Identifier: CA375788970

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695405C>T (hg19) ; chr9:g.137800953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800953C>T , CM000671.2:g.137800953C>T	GRCh38
NC_000009.11:g.140695405C>T , CM000671.1:g.140695405C>T	GRCh37
NC_000009.10:g.139815226C>T	NCBI36
NG_011776.1:g.186962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2681C>T MANE Select	ENSP00000417980.1:p.Ser894Phe
ENST00000636027.1:c.2567C>T	ENSP00000489961.1:p.Ser856Phe
ENST00000637161.1:c.2588C>T	ENSP00000490328.1:p.Ser863Phe
ENST00000637261.1:c.2721C>T	ENSP00000490815.1:n.2721C>T
ENST00000637891.1:c.575C>T	ENSP00000490907.1:p.Ser192Phe
ENST00000637949.1:c.359C>T	ENSP00000489786.1:p.Ser120Phe
ENST00000460843.5:c.2681C>T	ENSP00000417980.1:p.Ser894Phe
ENST00000462942.3:c.1538C>T	ENSP00000436107.1:p.Ser513Phe
ENST00000482340.5:c.251C>T	ENSP00000486748.1:p.Ser84Phe
ENST00000486164.5:c.259C>T
ENST00000488242.2:n.207C>T
ENST00000493484.5:c.251C>T	ENSP00000486503.1:p.Ser84Phe
NM_024757.4:c.2681C>T	NP_079033.4:p.Ser894Phe
XM_005266105.3:c.2672C>T	XP_005266162.1:p.Ser891Phe
XM_005266110.1:c.2588C>T	XP_005266167.1:p.Ser863Phe
XM_006717288.2:c.2663C>T	XP_006717351.1:p.Ser888Phe
XM_011519021.1:c.2690C>T	XP_011517323.1:p.Ser897Phe
XM_011519022.1:c.2687C>T	XP_011517324.1:p.Ser896Phe
XM_011519023.1:c.2669C>T	XP_011517325.1:p.Ser890Phe
XM_011519024.1:c.2612C>T	XP_011517326.1:p.Ser871Phe
XM_011519025.1:c.2588C>T	XP_011517327.1:p.Ser863Phe
XM_011519026.1:c.2546C>T	XP_011517328.1:p.Ser849Phe
XM_011519027.1:c.2690C>T	XP_011517329.1:p.Ser897Phe
XM_011519029.1:c.1112C>T	XP_011517331.1:p.Ser371Phe
XM_011519030.1:c.464C>T	XP_011517332.1:p.Ser155Phe
XM_011519031.1:c.251C>T	XP_011517333.1:p.Ser84Phe
XM_011519032.1:c.251C>T	XP_011517334.1:p.Ser84Phe
XM_011519033.1:c.2525C>T	XP_011517335.1:p.Ser842Phe
NM_001354263.1:c.2660C>T	NP_001341192.1:p.Ser887Phe
XM_005266105.5:c.2672C>T	XP_005266162.1:p.Ser891Phe
XM_011519021.3:c.2690C>T	XP_011517323.1:p.Ser897Phe
XM_011519022.3:c.2687C>T	XP_011517324.1:p.Ser896Phe
XM_011519023.3:c.2669C>T	XP_011517325.1:p.Ser890Phe
XM_011519029.3:c.1112C>T	XP_011517331.1:p.Ser371Phe
XM_011519030.3:c.464C>T	XP_011517332.1:p.Ser155Phe
XM_017015134.1:c.2666C>T	XP_016870623.1:p.Ser889Phe
XM_017015136.2:c.2582C>T	XP_016870625.1:p.Ser861Phe
XM_017015137.1:c.2567C>T	XP_016870626.1:p.Ser856Phe
XM_017015138.1:c.2567C>T	XP_016870627.1:p.Ser856Phe
XM_024447674.1:c.2510C>T	XP_024303442.1:p.Ser837Phe
XM_024447675.1:c.2444C>T	XP_024303443.1:p.Ser815Phe
XM_024447676.1:c.1805C>T	XP_024303444.1:p.Ser602Phe
XM_024447677.1:c.1805C>T	XP_024303445.1:p.Ser602Phe
XM_024447678.1:c.2588C>T	XP_024303446.1:p.Ser863Phe
XM_024447680.1:c.2423C>T	XP_024303448.1:p.Ser808Phe
NM_024757.5:c.2681C>T MANE Select	NP_079033.4:p.Ser894Phe
NM_001354263.2:c.2660C>T	NP_001341192.1:p.Ser887Phe