Canonical Allele Identifier: CA467877662

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140695412C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137800960C>A , CM000671.2:g.137800960C>A	GRCh38
NC_000009.11:g.140695412C>A , CM000671.1:g.140695412C>A	GRCh37
NC_000009.10:g.139815233C>A	NCBI36
NG_011776.1:g.186969C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460843.6:c.2688C>A MANE Select	ENSP00000417980.1:p.Gly896=
ENST00000636027.1:c.2574C>A	ENSP00000489961.1:p.Gly858=
ENST00000637161.1:c.2595C>A	ENSP00000490328.1:p.Gly865=
ENST00000637261.1:c.2728C>A	ENSP00000490815.1:n.2728C>A
ENST00000637891.1:c.582C>A	ENSP00000490907.1:p.Gly194=
ENST00000637949.1:c.366C>A	ENSP00000489786.1:p.Gly122=
ENST00000460843.5:c.2688C>A	ENSP00000417980.1:p.Gly896=
ENST00000462942.3:c.1545C>A	ENSP00000436107.1:p.Gly515=
ENST00000482340.5:c.258C>A	ENSP00000486748.1:p.Gly86=
ENST00000486164.5:c.266C>A
ENST00000488242.2:n.214C>A
ENST00000493484.5:c.258C>A	ENSP00000486503.1:p.Gly86=
NM_024757.4:c.2688C>A	NP_079033.4:p.Gly896=
XM_005266105.3:c.2679C>A	XP_005266162.1:p.Gly893=
XM_005266110.1:c.2595C>A	XP_005266167.1:p.Gly865=
XM_006717288.2:c.2670C>A	XP_006717351.1:p.Gly890=
XM_011519021.1:c.2697C>A	XP_011517323.1:p.Gly899=
XM_011519022.1:c.2694C>A	XP_011517324.1:p.Gly898=
XM_011519023.1:c.2676C>A	XP_011517325.1:p.Gly892=
XM_011519024.1:c.2619C>A	XP_011517326.1:p.Gly873=
XM_011519025.1:c.2595C>A	XP_011517327.1:p.Gly865=
XM_011519026.1:c.2553C>A	XP_011517328.1:p.Gly851=
XM_011519027.1:c.2697C>A	XP_011517329.1:p.Gly899=
XM_011519029.1:c.1119C>A	XP_011517331.1:p.Gly373=
XM_011519030.1:c.471C>A	XP_011517332.1:p.Gly157=
XM_011519031.1:c.258C>A	XP_011517333.1:p.Gly86=
XM_011519032.1:c.258C>A	XP_011517334.1:p.Gly86=
XM_011519033.1:c.2532C>A	XP_011517335.1:p.Gly844=
NM_001354263.1:c.2667C>A	NP_001341192.1:p.Gly889=
XM_005266105.5:c.2679C>A	XP_005266162.1:p.Gly893=
XM_011519021.3:c.2697C>A	XP_011517323.1:p.Gly899=
XM_011519022.3:c.2694C>A	XP_011517324.1:p.Gly898=
XM_011519023.3:c.2676C>A	XP_011517325.1:p.Gly892=
XM_011519029.3:c.1119C>A	XP_011517331.1:p.Gly373=
XM_011519030.3:c.471C>A	XP_011517332.1:p.Gly157=
XM_017015134.1:c.2673C>A	XP_016870623.1:p.Gly891=
XM_017015136.2:c.2589C>A	XP_016870625.1:p.Gly863=
XM_017015137.1:c.2574C>A	XP_016870626.1:p.Gly858=
XM_017015138.1:c.2574C>A	XP_016870627.1:p.Gly858=
XM_024447674.1:c.2517C>A	XP_024303442.1:p.Gly839=
XM_024447675.1:c.2451C>A	XP_024303443.1:p.Gly817=
XM_024447676.1:c.1812C>A	XP_024303444.1:p.Gly604=
XM_024447677.1:c.1812C>A	XP_024303445.1:p.Gly604=
XM_024447678.1:c.2595C>A	XP_024303446.1:p.Gly865=
XM_024447680.1:c.2430C>A	XP_024303448.1:p.Gly810=
NM_024757.5:c.2688C>A MANE Select	NP_079033.4:p.Gly896=
NM_001354263.2:c.2667C>A	NP_001341192.1:p.Gly889=