Canonical Allele Identifier: CA413449349

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69255227C>A (hg19) ; chrX:g.70035377C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035377C>A , CM000685.2:g.70035377C>A	GRCh38
NC_000023.10:g.69255227C>A , CM000685.1:g.69255227C>A	GRCh37
NC_000023.9:g.69171952C>A	NCBI36
NG_009809.1:g.424317C>A
NG_009809.2:g.424311C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.944C>A MANE Select	ENSP00000363680.4:p.Thr315Asn
ENST00000374552.8:c.944C>A	ENSP00000363680.4:p.Thr315Asn
ENST00000374553.6:c.938C>A	ENSP00000363681.2:p.Thr313Asn
ENST00000524573.5:c.929C>A	ENSP00000432585.1:p.Thr310Asn
ENST00000616899.1:c.548C>A	ENSP00000481963.1:p.Thr183Asn
NM_001005609.1:c.938C>A	NP_001005609.1:p.Thr313Asn
NM_001005612.2:c.929C>A	NP_001005612.2:p.Thr310Asn
NM_001399.4:c.944C>A	NP_001390.1:p.Thr315Asn
XM_006724630.2:c.935C>A	XP_006724693.1:p.Thr312Asn
XM_017029336.1:c.902C>A	XP_016884825.1:p.Thr301Asn
NM_001399.5:c.944C>A MANE Select	NP_001390.1:p.Thr315Asn
NM_001005609.2:c.938C>A	NP_001005609.1:p.Thr313Asn
NM_001005612.3:c.929C>A	NP_001005612.2:p.Thr310Asn