Canonical Allele Identifier: CA2435981940

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035478G= , CM000685.2:g.70035478G=	GRCh38
NC_000023.10:g.69255328G= , CM000685.1:g.69255328G=	GRCh37
NC_000023.9:g.69172053G=	NCBI36
NG_009809.1:g.424418G=
NG_009809.2:g.424412G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.1045G= MANE Select	NP_001390.1:p.Ala349=
ENST00000374552.9:c.1045G= MANE Select	ENSP00000363680.4:p.Ala349=
NM_001005609.1:c.1039G=	NP_001005609.1:p.Ala347=
NM_001005609.2:c.1039G=	NP_001005609.1:p.Ala347=
NM_001005612.2:c.1030G=	NP_001005612.2:p.Ala344=
NM_001005612.3:c.1030G=	NP_001005612.2:p.Ala344=
NM_001399.4:c.1045G=	NP_001390.1:p.Ala349=
ENST00000374552.8:c.1045G=	ENSP00000363680.4:p.Ala349=
ENST00000374553.6:c.1039G=	ENSP00000363681.2:p.Ala347=
ENST00000524573.5:c.1030G=	ENSP00000432585.1:p.Ala344=
ENST00000616899.1:c.649G=	ENSP00000481963.1:p.Ala217=
XM_006724630.2:c.1036G=	XP_006724693.1:p.Ala346=
XM_017029336.1:c.1003G=	XP_016884825.1:p.Ala335=