Canonical Allele Identifier: CA413448710

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69250356T>C (hg19) ; chrX:g.70030506T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70030506T>C , CM000685.2:g.70030506T>C	GRCh38
NC_000023.10:g.69250356T>C , CM000685.1:g.69250356T>C	GRCh37
NC_000023.9:g.69167081T>C	NCBI36
NG_009809.1:g.419446T>C
NG_009809.2:g.419440T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.779T>C MANE Select	ENSP00000363680.4:p.Ile260Thr
ENST00000374552.8:c.779T>C	ENSP00000363680.4:p.Ile260Thr
ENST00000374553.6:c.779T>C	ENSP00000363681.2:p.Ile260Thr
ENST00000503592.5:c.383T>C	ENSP00000423037.1:p.Ile128Thr
ENST00000524573.5:c.779T>C	ENSP00000432585.1:p.Ile260Thr
ENST00000616899.1:c.383T>C	ENSP00000481963.1:p.Ile128Thr
NM_001005609.1:c.779T>C	NP_001005609.1:p.Ile260Thr
NM_001005612.2:c.779T>C	NP_001005612.2:p.Ile260Thr
NM_001399.4:c.779T>C	NP_001390.1:p.Ile260Thr
XM_006724630.2:c.779T>C	XP_006724693.1:p.Ile260Thr
XM_011530885.1:c.779T>C	XP_011529187.1:p.Ile260Thr
XM_011530885.2:c.779T>C	XP_011529187.1:p.Ile260Thr
XM_017029336.1:c.779T>C	XP_016884825.1:p.Ile260Thr
NM_001399.5:c.779T>C MANE Select	NP_001390.1:p.Ile260Thr
NM_001005609.2:c.779T>C	NP_001005609.1:p.Ile260Thr
NM_001005612.3:c.779T>C	NP_001005612.2:p.Ile260Thr