Canonical Allele Identifier: CA413449015

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69253362T>A (hg19) ; chrX:g.70033512T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033512T>A , CM000685.2:g.70033512T>A	GRCh38
NC_000023.10:g.69253362T>A , CM000685.1:g.69253362T>A	GRCh37
NC_000023.9:g.69170087T>A	NCBI36
NG_009809.1:g.422452T>A
NG_009809.2:g.422446T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.908T>A MANE Select	ENSP00000363680.4:p.Ile303Asn
ENST00000374552.8:c.908T>A	ENSP00000363680.4:p.Ile303Asn
ENST00000374553.6:c.908T>A	ENSP00000363681.2:p.Ile303Asn
ENST00000524573.5:c.899T>A	ENSP00000432585.1:p.Ile300Asn
ENST00000616899.1:c.512T>A	ENSP00000481963.1:p.Ile171Asn
NM_001005609.1:c.908T>A	NP_001005609.1:p.Ile303Asn
NM_001005612.2:c.899T>A	NP_001005612.2:p.Ile300Asn
NM_001399.4:c.908T>A	NP_001390.1:p.Ile303Asn
XM_006724630.2:c.899T>A	XP_006724693.1:p.Ile300Asn
XM_011530885.1:c.908T>A	XP_011529187.1:p.Ile303Asn
XM_011530885.2:c.908T>A	XP_011529187.1:p.Ile303Asn
XM_017029336.1:c.882+26T>A	XP_016884825.1:n.882+26T>A
NM_001399.5:c.908T>A MANE Select	NP_001390.1:p.Ile303Asn
NM_001005609.2:c.908T>A	NP_001005609.1:p.Ile303Asn
NM_001005612.3:c.899T>A	NP_001005612.2:p.Ile300Asn