Canonical Allele Identifier: CA2435981879

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035321T= , CM000685.2:g.70035321T=	GRCh38
NC_000023.10:g.69255171T= , CM000685.1:g.69255171T=	GRCh37
NC_000023.9:g.69171896T=	NCBI36
NG_009809.1:g.424261T=
NG_009809.2:g.424255T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.925-37T= MANE Select	ENSP00000363680.4:n.925-37T=
ENST00000374552.8:c.925-37T=	ENSP00000363680.4:n.925-37T=
ENST00000374553.6:c.919-37T=	ENSP00000363681.2:n.919-37T=
ENST00000524573.5:c.910-37T=	ENSP00000432585.1:n.910-37T=
ENST00000616899.1:c.529-37T=	ENSP00000481963.1:n.529-37T=
NM_001005609.1:c.919-37T=	NP_001005609.1:n.919-37T=
NM_001005612.2:c.910-37T=	NP_001005612.2:n.910-37T=
NM_001399.4:c.925-37T=	NP_001390.1:n.925-37T=
XM_006724630.2:c.916-37T=	XP_006724693.1:n.916-37T=
XM_017029336.1:c.883-37T=	XP_016884825.1:n.883-37T=
NM_001399.5:c.925-37T= MANE Select	NP_001390.1:n.925-37T=
NM_001005609.2:c.919-37T=	NP_001005609.1:n.919-37T=
NM_001005612.3:c.910-37T=	NP_001005612.2:n.910-37T=