Canonical Allele Identifier: CA2435981895

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035365A= , CM000685.2:g.70035365A=	GRCh38
NC_000023.10:g.69255215A= , CM000685.1:g.69255215A=	GRCh37
NC_000023.9:g.69171940A=	NCBI36
NG_009809.1:g.424305A=
NG_009809.2:g.424299A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001399.5:c.932A= MANE Select	NP_001390.1:p.Tyr311=
ENST00000374552.9:c.932A= MANE Select	ENSP00000363680.4:p.Tyr311=
NM_001005609.1:c.926A=	NP_001005609.1:p.Tyr309=
NM_001005609.2:c.926A=	NP_001005609.1:p.Tyr309=
NM_001005612.2:c.917A=	NP_001005612.2:p.Tyr306=
NM_001005612.3:c.917A=	NP_001005612.2:p.Tyr306=
NM_001399.4:c.932A=	NP_001390.1:p.Tyr311=
ENST00000374552.8:c.932A=	ENSP00000363680.4:p.Tyr311=
ENST00000374553.6:c.926A=	ENSP00000363681.2:p.Tyr309=
ENST00000524573.5:c.917A=	ENSP00000432585.1:p.Tyr306=
ENST00000616899.1:c.536A=	ENSP00000481963.1:p.Tyr179=
XM_006724630.2:c.923A=	XP_006724693.1:p.Tyr308=
XM_017029336.1:c.890A=	XP_016884825.1:p.Tyr297=