Canonical Allele Identifier: CA2435981899

Gene: EDA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035374T= , CM000685.2:g.70035374T=	GRCh38
NC_000023.10:g.69255224T= , CM000685.1:g.69255224T=	GRCh37
NC_000023.9:g.69171949T=	NCBI36
NG_009809.1:g.424314T=
NG_009809.2:g.424308T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.941T= MANE Select	ENSP00000363680.4:p.Phe314=
ENST00000374552.8:c.941T=	ENSP00000363680.4:p.Phe314=
ENST00000374553.6:c.935T=	ENSP00000363681.2:p.Phe312=
ENST00000524573.5:c.926T=	ENSP00000432585.1:p.Phe309=
ENST00000616899.1:c.545T=	ENSP00000481963.1:p.Phe182=
NM_001005609.1:c.935T=	NP_001005609.1:p.Phe312=
NM_001005612.2:c.926T=	NP_001005612.2:p.Phe309=
NM_001399.4:c.941T=	NP_001390.1:p.Phe314=
XM_006724630.2:c.932T=	XP_006724693.1:p.Phe311=
XM_017029336.1:c.899T=	XP_016884825.1:p.Phe300=
NM_001399.5:c.941T= MANE Select	NP_001390.1:p.Phe314=
NM_001005609.2:c.935T=	NP_001005609.1:p.Phe312=
NM_001005612.3:c.926T=	NP_001005612.2:p.Phe309=