Canonical Allele Identifier: CA2435981894

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035364T= , CM000685.2:g.70035364T=	GRCh38
NC_000023.10:g.69255214T= , CM000685.1:g.69255214T=	GRCh37
NC_000023.9:g.69171939T=	NCBI36
NG_009809.1:g.424304T=
NG_009809.2:g.424298T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.931T= MANE Select	ENSP00000363680.4:p.Tyr311=
ENST00000374552.8:c.931T=	ENSP00000363680.4:p.Tyr311=
ENST00000374553.6:c.925T=	ENSP00000363681.2:p.Tyr309=
ENST00000524573.5:c.916T=	ENSP00000432585.1:p.Tyr306=
ENST00000616899.1:c.535T=	ENSP00000481963.1:p.Tyr179=
NM_001005609.1:c.925T=	NP_001005609.1:p.Tyr309=
NM_001005612.2:c.916T=	NP_001005612.2:p.Tyr306=
NM_001399.4:c.931T=	NP_001390.1:p.Tyr311=
XM_006724630.2:c.922T=	XP_006724693.1:p.Tyr308=
XM_017029336.1:c.889T=	XP_016884825.1:p.Tyr297=
NM_001399.5:c.931T= MANE Select	NP_001390.1:p.Tyr311=
NM_001005609.2:c.925T=	NP_001005609.1:p.Tyr309=
NM_001005612.3:c.916T=	NP_001005612.2:p.Tyr306=