Canonical Allele Identifier: CA468161032

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707482T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813030T>C , CM000671.2:g.137813030T>C	GRCh38
NC_000009.11:g.140707482T>C , CM000671.1:g.140707482T>C	GRCh37
NC_000009.10:g.139827303T>C	NCBI36
NG_011776.1:g.199039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2892T>C MANE Select	ENSP00000417980.1:p.Asp964=
ENST00000636027.1:c.2778T>C	ENSP00000489961.1:p.Asp926=
ENST00000637161.1:c.2799T>C	ENSP00000490328.1:p.Asp933=
ENST00000637261.1:c.2932T>C	ENSP00000490815.1:n.2932T>C
ENST00000637891.1:c.786T>C	ENSP00000490907.1:p.Asp262=
ENST00000460843.5:c.2892T>C	ENSP00000417980.1:p.Asp964=
ENST00000462942.3:c.1749T>C	ENSP00000436107.1:p.Asp583=
ENST00000486164.5:c.579T>C
ENST00000488242.2:n.418T>C
NM_024757.4:c.2892T>C	NP_079033.4:p.Asp964=
XM_005266105.3:c.2883T>C	XP_005266162.1:p.Asp961=
XM_005266110.1:c.2799T>C	XP_005266167.1:p.Asp933=
XM_006717288.2:c.2874T>C	XP_006717351.1:p.Asp958=
XM_011519021.1:c.2901T>C	XP_011517323.1:p.Asp967=
XM_011519022.1:c.2898T>C	XP_011517324.1:p.Asp966=
XM_011519023.1:c.2880T>C	XP_011517325.1:p.Asp960=
XM_011519024.1:c.2823T>C	XP_011517326.1:p.Asp941=
XM_011519025.1:c.2799T>C	XP_011517327.1:p.Asp933=
XM_011519026.1:c.2757T>C	XP_011517328.1:p.Asp919=
XM_011519029.1:c.1323T>C	XP_011517331.1:p.Asp441=
XM_011519030.1:c.675T>C	XP_011517332.1:p.Asp225=
XM_011519031.1:c.462T>C	XP_011517333.1:p.Asp154=
XM_011519032.1:c.462T>C	XP_011517334.1:p.Asp154=
XM_011519033.1:c.2736T>C	XP_011517335.1:p.Asp912=
NM_001354263.1:c.2871T>C	NP_001341192.1:p.Asp957=
XM_005266105.5:c.2883T>C	XP_005266162.1:p.Asp961=
XM_011519021.3:c.2901T>C	XP_011517323.1:p.Asp967=
XM_011519022.3:c.2898T>C	XP_011517324.1:p.Asp966=
XM_011519023.3:c.2880T>C	XP_011517325.1:p.Asp960=
XM_011519029.3:c.1323T>C	XP_011517331.1:p.Asp441=
XM_011519030.3:c.675T>C	XP_011517332.1:p.Asp225=
XM_017015134.1:c.2877T>C	XP_016870623.1:p.Asp959=
XM_017015136.2:c.2793T>C	XP_016870625.1:p.Asp931=
XM_017015137.1:c.2778T>C	XP_016870626.1:p.Asp926=
XM_017015138.1:c.2778T>C	XP_016870627.1:p.Asp926=
XM_024447674.1:c.2721T>C	XP_024303442.1:p.Asp907=
XM_024447675.1:c.2655T>C	XP_024303443.1:p.Asp885=
XM_024447676.1:c.2016T>C	XP_024303444.1:p.Asp672=
XM_024447677.1:c.2016T>C	XP_024303445.1:p.Asp672=
XM_024447680.1:c.2634T>C	XP_024303448.1:p.Asp878=
NM_024757.5:c.2892T>C MANE Select	NP_079033.4:p.Asp964=
NM_001354263.2:c.2871T>C	NP_001341192.1:p.Asp957=