Canonical Allele Identifier: CA375793655

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707580A>T (hg19) ; chr9:g.137813128A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813128A>T , CM000671.2:g.137813128A>T	GRCh38
NC_000009.11:g.140707580A>T , CM000671.1:g.140707580A>T	GRCh37
NC_000009.10:g.139827401A>T	NCBI36
NG_011776.1:g.199137A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2990A>T MANE Select	ENSP00000417980.1:p.Asp997Val
ENST00000636027.1:c.2876A>T	ENSP00000489961.1:p.Asp959Val
ENST00000637161.1:c.2897A>T	ENSP00000490328.1:p.Asp966Val
ENST00000637261.1:c.3030A>T	ENSP00000490815.1:n.3030A>T
ENST00000637891.1:c.884A>T	ENSP00000490907.1:p.Asp295Val
ENST00000460843.5:c.2990A>T	ENSP00000417980.1:p.Asp997Val
ENST00000462942.3:c.1847A>T	ENSP00000436107.1:p.Asp616Val
ENST00000486164.5:c.677A>T
ENST00000488242.2:n.516A>T
NM_024757.4:c.2990A>T	NP_079033.4:p.Asp997Val
XM_005266105.3:c.2981A>T	XP_005266162.1:p.Asp994Val
XM_005266110.1:c.2897A>T	XP_005266167.1:p.Asp966Val
XM_006717288.2:c.2972A>T	XP_006717351.1:p.Asp991Val
XM_011519021.1:c.2999A>T	XP_011517323.1:p.Asp1000Val
XM_011519022.1:c.2996A>T	XP_011517324.1:p.Asp999Val
XM_011519023.1:c.2978A>T	XP_011517325.1:p.Asp993Val
XM_011519024.1:c.2921A>T	XP_011517326.1:p.Asp974Val
XM_011519025.1:c.2897A>T	XP_011517327.1:p.Asp966Val
XM_011519026.1:c.2855A>T	XP_011517328.1:p.Asp952Val
XM_011519029.1:c.1421A>T	XP_011517331.1:p.Asp474Val
XM_011519030.1:c.773A>T	XP_011517332.1:p.Asp258Val
XM_011519031.1:c.560A>T	XP_011517333.1:p.Asp187Val
XM_011519032.1:c.560A>T	XP_011517334.1:p.Asp187Val
XM_011519033.1:c.2834A>T	XP_011517335.1:p.Asp945Val
NM_001354263.1:c.2969A>T	NP_001341192.1:p.Asp990Val
XM_005266105.5:c.2981A>T	XP_005266162.1:p.Asp994Val
XM_011519021.3:c.2999A>T	XP_011517323.1:p.Asp1000Val
XM_011519022.3:c.2996A>T	XP_011517324.1:p.Asp999Val
XM_011519023.3:c.2978A>T	XP_011517325.1:p.Asp993Val
XM_011519029.3:c.1421A>T	XP_011517331.1:p.Asp474Val
XM_011519030.3:c.773A>T	XP_011517332.1:p.Asp258Val
XM_017015134.1:c.2975A>T	XP_016870623.1:p.Asp992Val
XM_017015136.2:c.2891A>T	XP_016870625.1:p.Asp964Val
XM_017015137.1:c.2876A>T	XP_016870626.1:p.Asp959Val
XM_017015138.1:c.2876A>T	XP_016870627.1:p.Asp959Val
XM_024447674.1:c.2819A>T	XP_024303442.1:p.Asp940Val
XM_024447675.1:c.2753A>T	XP_024303443.1:p.Asp918Val
XM_024447676.1:c.2114A>T	XP_024303444.1:p.Asp705Val
XM_024447677.1:c.2114A>T	XP_024303445.1:p.Asp705Val
XM_024447680.1:c.2732A>T	XP_024303448.1:p.Asp911Val
NM_024757.5:c.2990A>T MANE Select	NP_079033.4:p.Asp997Val
NM_001354263.2:c.2969A>T	NP_001341192.1:p.Asp990Val