Canonical Allele Identifier: CA2435981269

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033346T= , CM000685.2:g.70033346T=	GRCh38
NC_000023.10:g.69253196T= , CM000685.1:g.69253196T=	GRCh37
NC_000023.9:g.69169921T=	NCBI36
NG_009809.1:g.422286T=
NG_009809.2:g.422280T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.794-52T= MANE Select	ENSP00000363680.4:n.794-52T=
ENST00000374552.8:c.794-52T=	ENSP00000363680.4:n.794-52T=
ENST00000374553.6:c.794-52T=	ENSP00000363681.2:n.794-52T=
ENST00000503592.5:c.398-52T=	ENSP00000423037.1:n.398-52T=
ENST00000524573.5:c.794-61T=	ENSP00000432585.1:n.794-61T=
ENST00000616899.1:c.398-52T=	ENSP00000481963.1:n.398-52T=
NM_001005609.1:c.794-52T=	NP_001005609.1:n.794-52T=
NM_001005612.2:c.794-61T=	NP_001005612.2:n.794-61T=
NM_001399.4:c.794-52T=	NP_001390.1:n.794-52T=
XM_006724630.2:c.794-61T=	XP_006724693.1:n.794-61T=
XM_011530885.1:c.794-52T=	XP_011529187.1:n.794-52T=
XM_011530885.2:c.794-52T=	XP_011529187.1:n.794-52T=
XM_017029336.1:c.794-52T=	XP_016884825.1:n.794-52T=
NM_001399.5:c.794-52T= MANE Select	NP_001390.1:n.794-52T=
NM_001005609.2:c.794-52T=	NP_001005609.1:n.794-52T=
NM_001005612.3:c.794-61T=	NP_001005612.2:n.794-61T=