Canonical Allele Identifier: CA375789018

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695419A>T (hg19) ; chr9:g.137800967A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800967A>T , CM000671.2:g.137800967A>T	GRCh38
NC_000009.11:g.140695419A>T , CM000671.1:g.140695419A>T	GRCh37
NC_000009.10:g.139815240A>T	NCBI36
NG_011776.1:g.186976A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2695A>T MANE Select	ENSP00000417980.1:p.Ile899Phe
ENST00000636027.1:c.2581A>T	ENSP00000489961.1:p.Ile861Phe
ENST00000637161.1:c.2602A>T	ENSP00000490328.1:p.Ile868Phe
ENST00000637261.1:c.2735A>T	ENSP00000490815.1:n.2735A>T
ENST00000637891.1:c.589A>T	ENSP00000490907.1:p.Ile197Phe
ENST00000637949.1:c.373A>T	ENSP00000489786.1:p.Ile125Phe
ENST00000460843.5:c.2695A>T	ENSP00000417980.1:p.Ile899Phe
ENST00000462942.3:c.1552A>T	ENSP00000436107.1:p.Ile518Phe
ENST00000482340.5:c.265A>T	ENSP00000486748.1:p.Ile89Phe
ENST00000486164.5:c.273A>T
ENST00000488242.2:n.221A>T
ENST00000493484.5:c.265A>T	ENSP00000486503.1:p.Ile89Phe
NM_024757.4:c.2695A>T	NP_079033.4:p.Ile899Phe
XM_005266105.3:c.2686A>T	XP_005266162.1:p.Ile896Phe
XM_005266110.1:c.2602A>T	XP_005266167.1:p.Ile868Phe
XM_006717288.2:c.2677A>T	XP_006717351.1:p.Ile893Phe
XM_011519021.1:c.2704A>T	XP_011517323.1:p.Ile902Phe
XM_011519022.1:c.2701A>T	XP_011517324.1:p.Ile901Phe
XM_011519023.1:c.2683A>T	XP_011517325.1:p.Ile895Phe
XM_011519024.1:c.2626A>T	XP_011517326.1:p.Ile876Phe
XM_011519025.1:c.2602A>T	XP_011517327.1:p.Ile868Phe
XM_011519026.1:c.2560A>T	XP_011517328.1:p.Ile854Phe
XM_011519027.1:c.2704A>T	XP_011517329.1:p.Ile902Phe
XM_011519029.1:c.1126A>T	XP_011517331.1:p.Ile376Phe
XM_011519030.1:c.478A>T	XP_011517332.1:p.Ile160Phe
XM_011519031.1:c.265A>T	XP_011517333.1:p.Ile89Phe
XM_011519032.1:c.265A>T	XP_011517334.1:p.Ile89Phe
XM_011519033.1:c.2539A>T	XP_011517335.1:p.Ile847Phe
NM_001354263.1:c.2674A>T	NP_001341192.1:p.Ile892Phe
XM_005266105.5:c.2686A>T	XP_005266162.1:p.Ile896Phe
XM_011519021.3:c.2704A>T	XP_011517323.1:p.Ile902Phe
XM_011519022.3:c.2701A>T	XP_011517324.1:p.Ile901Phe
XM_011519023.3:c.2683A>T	XP_011517325.1:p.Ile895Phe
XM_011519029.3:c.1126A>T	XP_011517331.1:p.Ile376Phe
XM_011519030.3:c.478A>T	XP_011517332.1:p.Ile160Phe
XM_017015134.1:c.2680A>T	XP_016870623.1:p.Ile894Phe
XM_017015136.2:c.2596A>T	XP_016870625.1:p.Ile866Phe
XM_017015137.1:c.2581A>T	XP_016870626.1:p.Ile861Phe
XM_017015138.1:c.2581A>T	XP_016870627.1:p.Ile861Phe
XM_024447674.1:c.2524A>T	XP_024303442.1:p.Ile842Phe
XM_024447675.1:c.2458A>T	XP_024303443.1:p.Ile820Phe
XM_024447676.1:c.1819A>T	XP_024303444.1:p.Ile607Phe
XM_024447677.1:c.1819A>T	XP_024303445.1:p.Ile607Phe
XM_024447678.1:c.2602A>T	XP_024303446.1:p.Ile868Phe
XM_024447680.1:c.2437A>T	XP_024303448.1:p.Ile813Phe
NM_024757.5:c.2695A>T MANE Select	NP_079033.4:p.Ile899Phe
NM_001354263.2:c.2674A>T	NP_001341192.1:p.Ile892Phe