Canonical Allele Identifier: CA468161014

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707458C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813006C>T , CM000671.2:g.137813006C>T	GRCh38
NC_000009.11:g.140707458C>T , CM000671.1:g.140707458C>T	GRCh37
NC_000009.10:g.139827279C>T	NCBI36
NG_011776.1:g.199015C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2868C>T MANE Select	ENSP00000417980.1:p.Val956=
ENST00000636027.1:c.2754C>T	ENSP00000489961.1:p.Val918=
ENST00000637161.1:c.2775C>T	ENSP00000490328.1:p.Val925=
ENST00000637261.1:c.2908C>T	ENSP00000490815.1:n.2908C>T
ENST00000637891.1:c.762C>T	ENSP00000490907.1:p.Val254=
ENST00000460843.5:c.2868C>T	ENSP00000417980.1:p.Val956=
ENST00000462942.3:c.1725C>T	ENSP00000436107.1:p.Val575=
ENST00000486164.5:c.555C>T
ENST00000488242.2:n.394C>T
NM_024757.4:c.2868C>T	NP_079033.4:p.Val956=
XM_005266105.3:c.2859C>T	XP_005266162.1:p.Val953=
XM_005266110.1:c.2775C>T	XP_005266167.1:p.Val925=
XM_006717288.2:c.2850C>T	XP_006717351.1:p.Val950=
XM_011519021.1:c.2877C>T	XP_011517323.1:p.Val959=
XM_011519022.1:c.2874C>T	XP_011517324.1:p.Val958=
XM_011519023.1:c.2856C>T	XP_011517325.1:p.Val952=
XM_011519024.1:c.2799C>T	XP_011517326.1:p.Val933=
XM_011519025.1:c.2775C>T	XP_011517327.1:p.Val925=
XM_011519026.1:c.2733C>T	XP_011517328.1:p.Val911=
XM_011519029.1:c.1299C>T	XP_011517331.1:p.Val433=
XM_011519030.1:c.651C>T	XP_011517332.1:p.Val217=
XM_011519031.1:c.438C>T	XP_011517333.1:p.Val146=
XM_011519032.1:c.438C>T	XP_011517334.1:p.Val146=
XM_011519033.1:c.2712C>T	XP_011517335.1:p.Val904=
NM_001354263.1:c.2847C>T	NP_001341192.1:p.Val949=
XM_005266105.5:c.2859C>T	XP_005266162.1:p.Val953=
XM_011519021.3:c.2877C>T	XP_011517323.1:p.Val959=
XM_011519022.3:c.2874C>T	XP_011517324.1:p.Val958=
XM_011519023.3:c.2856C>T	XP_011517325.1:p.Val952=
XM_011519029.3:c.1299C>T	XP_011517331.1:p.Val433=
XM_011519030.3:c.651C>T	XP_011517332.1:p.Val217=
XM_017015134.1:c.2853C>T	XP_016870623.1:p.Val951=
XM_017015136.2:c.2769C>T	XP_016870625.1:p.Val923=
XM_017015137.1:c.2754C>T	XP_016870626.1:p.Val918=
XM_017015138.1:c.2754C>T	XP_016870627.1:p.Val918=
XM_024447674.1:c.2697C>T	XP_024303442.1:p.Val899=
XM_024447675.1:c.2631C>T	XP_024303443.1:p.Val877=
XM_024447676.1:c.1992C>T	XP_024303444.1:p.Val664=
XM_024447677.1:c.1992C>T	XP_024303445.1:p.Val664=
XM_024447680.1:c.2610C>T	XP_024303448.1:p.Val870=
NM_024757.5:c.2868C>T MANE Select	NP_079033.4:p.Val956=
NM_001354263.2:c.2847C>T	NP_001341192.1:p.Val949=