Canonical Allele Identifier: CA2435981931

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035446C= , CM000685.2:g.70035446C=	GRCh38
NC_000023.10:g.69255296C= , CM000685.1:g.69255296C=	GRCh37
NC_000023.9:g.69172021C=	NCBI36
NG_009809.1:g.424386C=
NG_009809.2:g.424380C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.1013C= MANE Select	NP_001390.1:p.Thr338=
ENST00000374552.9:c.1013C= MANE Select	ENSP00000363680.4:p.Thr338=
NM_001005609.1:c.1007C=	NP_001005609.1:p.Thr336=
NM_001005609.2:c.1007C=	NP_001005609.1:p.Thr336=
NM_001005612.2:c.998C=	NP_001005612.2:p.Thr333=
NM_001005612.3:c.998C=	NP_001005612.2:p.Thr333=
NM_001399.4:c.1013C=	NP_001390.1:p.Thr338=
ENST00000374552.8:c.1013C=	ENSP00000363680.4:p.Thr338=
ENST00000374553.6:c.1007C=	ENSP00000363681.2:p.Thr336=
ENST00000524573.5:c.998C=	ENSP00000432585.1:p.Thr333=
ENST00000616899.1:c.617C=	ENSP00000481963.1:p.Thr206=
XM_006724630.2:c.1004C=	XP_006724693.1:p.Thr335=
XM_017029336.1:c.971C=	XP_016884825.1:p.Thr324=