Canonical Allele Identifier: CA2435981957

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035527T= , CM000685.2:g.70035527T=	GRCh38
NC_000023.10:g.69255377T= , CM000685.1:g.69255377T=	GRCh37
NC_000023.9:g.69172102T=	NCBI36
NG_009809.1:g.424467T=
NG_009809.2:g.424461T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.1094T= MANE Select	ENSP00000363680.4:p.Val365=
ENST00000374552.8:c.1094T=	ENSP00000363680.4:p.Val365=
ENST00000374553.6:c.1088T=	ENSP00000363681.2:p.Val363=
ENST00000524573.5:c.1079T=	ENSP00000432585.1:p.Val360=
ENST00000616899.1:c.698T=	ENSP00000481963.1:p.Val233=
NM_001005609.1:c.1088T=	NP_001005609.1:p.Val363=
NM_001005612.2:c.1079T=	NP_001005612.2:p.Val360=
NM_001399.4:c.1094T=	NP_001390.1:p.Val365=
XM_006724630.2:c.1085T=	XP_006724693.1:p.Val362=
XM_017029336.1:c.1052T=	XP_016884825.1:p.Val351=
NM_001399.5:c.1094T= MANE Select	NP_001390.1:p.Val365=
NM_001005609.2:c.1088T=	NP_001005609.1:p.Val363=
NM_001005612.3:c.1079T=	NP_001005612.2:p.Val360=