Canonical Allele Identifier: CA413448826

Gene: EDA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033431G>A , CM000685.2:g.70033431G>A	GRCh38
NC_000023.10:g.69253281G>A , CM000685.1:g.69253281G>A	GRCh37
NC_000023.9:g.69170006G>A	NCBI36
NG_009809.1:g.422371G>A
NG_009809.2:g.422365G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.827G>A MANE Select	ENSP00000363680.4:p.Arg276His
ENST00000374552.8:c.827G>A	ENSP00000363680.4:p.Arg276His
ENST00000374553.6:c.827G>A	ENSP00000363681.2:p.Arg276His
ENST00000524573.5:c.818G>A	ENSP00000432585.1:p.Arg273His
ENST00000616899.1:c.431G>A	ENSP00000481963.1:p.Arg144His
NM_001005609.1:c.827G>A	NP_001005609.1:p.Arg276His
NM_001005612.2:c.818G>A	NP_001005612.2:p.Arg273His
NM_001399.4:c.827G>A	NP_001390.1:p.Arg276His
XM_006724630.2:c.818G>A	XP_006724693.1:p.Arg273His
XM_011530885.1:c.827G>A	XP_011529187.1:p.Arg276His
XM_011530885.2:c.827G>A	XP_011529187.1:p.Arg276His
XM_017029336.1:c.827G>A	XP_016884825.1:p.Arg276His
NM_001399.5:c.827G>A MANE Select	NP_001390.1:p.Arg276His
NM_001005609.2:c.827G>A	NP_001005609.1:p.Arg276His
NM_001005612.3:c.818G>A	NP_001005612.2:p.Arg273His