Canonical Allele Identifier: CA2435981898

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035369C= , CM000685.2:g.70035369C=	GRCh38
NC_000023.10:g.69255219C= , CM000685.1:g.69255219C=	GRCh37
NC_000023.9:g.69171944C=	NCBI36
NG_009809.1:g.424309C=
NG_009809.2:g.424303C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.936C= MANE Select	ENSP00000363680.4:p.Ile312=
ENST00000374552.8:c.936C=	ENSP00000363680.4:p.Ile312=
ENST00000374553.6:c.930C=	ENSP00000363681.2:p.Ile310=
ENST00000524573.5:c.921C=	ENSP00000432585.1:p.Ile307=
ENST00000616899.1:c.540C=	ENSP00000481963.1:p.Ile180=
NM_001005609.1:c.930C=	NP_001005609.1:p.Ile310=
NM_001005612.2:c.921C=	NP_001005612.2:p.Ile307=
NM_001399.4:c.936C=	NP_001390.1:p.Ile312=
XM_006724630.2:c.927C=	XP_006724693.1:p.Ile309=
XM_017029336.1:c.894C=	XP_016884825.1:p.Ile298=
NM_001399.5:c.936C= MANE Select	NP_001390.1:p.Ile312=
NM_001005609.2:c.930C=	NP_001005609.1:p.Ile310=
NM_001005612.3:c.921C=	NP_001005612.2:p.Ile307=