Canonical Allele Identifier: CA375793976

Gene: EHMT1

Linked Data

• MyVariant Identifiers: chr9:g.140707881A>C (hg19) ; chr9:g.137813429A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.137813429A>C , CM000671.2:g.137813429A>C	GRCh38
NC_000009.11:g.140707881A>C , CM000671.1:g.140707881A>C	GRCh37
NC_000009.10:g.139827702A>C	NCBI36
NG_011776.1:g.199438A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000460843.6:c.3079A>C MANE Select	ENSP00000417980.1:p.Asn1027His
ENST00000637161.1:c.2986A>C	ENSP00000490328.1:p.Asn996His
ENST00000637261.1:c.3119A>C	ENSP00000490815.1:n.3119A>C
ENST00000637891.1:c.973A>C	ENSP00000490907.1:p.Asn325His
ENST00000460843.5:c.3079A>C	ENSP00000417980.1:p.Asn1027His
ENST00000462942.3:c.1936A>C	ENSP00000436107.1:p.Asn646His
ENST00000486164.5:c.766A>C
ENST00000488242.2:n.605A>C
NM_024757.4:c.3079A>C	NP_079033.4:p.Asn1027His
XM_005266105.3:c.3070A>C	XP_005266162.1:p.Asn1024His
XM_005266110.1:c.2986A>C	XP_005266167.1:p.Asn996His
XM_006717288.2:c.3061A>C	XP_006717351.1:p.Asn1021His
XM_011519021.1:c.3088A>C	XP_011517323.1:p.Asn1030His
XM_011519022.1:c.3085A>C	XP_011517324.1:p.Asn1029His
XM_011519023.1:c.3067A>C	XP_011517325.1:p.Asn1023His
XM_011519024.1:c.3010A>C	XP_011517326.1:p.Asn1004His
XM_011519025.1:c.2986A>C	XP_011517327.1:p.Asn996His
XM_011519026.1:c.2944A>C	XP_011517328.1:p.Asn982His
XM_011519029.1:c.1510A>C	XP_011517331.1:p.Asn504His
XM_011519030.1:c.862A>C	XP_011517332.1:p.Asn288His
XM_011519031.1:c.649A>C	XP_011517333.1:p.Asn217His
XM_011519032.1:c.649A>C	XP_011517334.1:p.Asn217His
XM_011519033.1:c.2923A>C	XP_011517335.1:p.Asn975His
NM_001354263.1:c.3058A>C	NP_001341192.1:p.Asn1020His
XM_005266105.5:c.3070A>C	XP_005266162.1:p.Asn1024His
XM_011519021.3:c.3088A>C	XP_011517323.1:p.Asn1030His
XM_011519022.3:c.3085A>C	XP_011517324.1:p.Asn1029His
XM_011519023.3:c.3067A>C	XP_011517325.1:p.Asn1023His
XM_011519029.3:c.1510A>C	XP_011517331.1:p.Asn504His
XM_011519030.3:c.862A>C	XP_011517332.1:p.Asn288His
XM_017015134.1:c.3064A>C	XP_016870623.1:p.Asn1022His
XM_017015136.2:c.2980A>C	XP_016870625.1:p.Asn994His
XM_017015137.1:c.2965A>C	XP_016870626.1:p.Asn989His
XM_017015138.1:c.2965A>C	XP_016870627.1:p.Asn989His
XM_024447674.1:c.2908A>C	XP_024303442.1:p.Asn970His
XM_024447675.1:c.2842A>C	XP_024303443.1:p.Asn948His
XM_024447676.1:c.2203A>C	XP_024303444.1:p.Asn735His
XM_024447677.1:c.2203A>C	XP_024303445.1:p.Asn735His
XM_024447680.1:c.2821A>C	XP_024303448.1:p.Asn941His
NM_024757.5:c.3079A>C MANE Select	NP_079033.4:p.Asn1027His
NM_001354263.2:c.3058A>C	NP_001341192.1:p.Asn1020His