Canonical Allele Identifier: CA413448994

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69253358T>A (hg19) ; chrX:g.70033508T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033508T>A , CM000685.2:g.70033508T>A	GRCh38
NC_000023.10:g.69253358T>A , CM000685.1:g.69253358T>A	GRCh37
NC_000023.9:g.69170083T>A	NCBI36
NG_009809.1:g.422448T>A
NG_009809.2:g.422442T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.904T>A MANE Select	ENSP00000363680.4:p.Phe302Ile
ENST00000374552.8:c.904T>A	ENSP00000363680.4:p.Phe302Ile
ENST00000374553.6:c.904T>A	ENSP00000363681.2:p.Phe302Ile
ENST00000524573.5:c.895T>A	ENSP00000432585.1:p.Phe299Ile
ENST00000616899.1:c.508T>A	ENSP00000481963.1:p.Phe170Ile
NM_001005609.1:c.904T>A	NP_001005609.1:p.Phe302Ile
NM_001005612.2:c.895T>A	NP_001005612.2:p.Phe299Ile
NM_001399.4:c.904T>A	NP_001390.1:p.Phe302Ile
XM_006724630.2:c.895T>A	XP_006724693.1:p.Phe299Ile
XM_011530885.1:c.904T>A	XP_011529187.1:p.Phe302Ile
XM_011530885.2:c.904T>A	XP_011529187.1:p.Phe302Ile
XM_017029336.1:c.882+22T>A	XP_016884825.1:n.882+22T>A
NM_001399.5:c.904T>A MANE Select	NP_001390.1:p.Phe302Ile
NM_001005609.2:c.904T>A	NP_001005609.1:p.Phe302Ile
NM_001005612.3:c.895T>A	NP_001005612.2:p.Phe299Ile