Canonical Allele Identifier: CA517013123

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69250351A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70030501A>G , CM000685.2:g.70030501A>G	GRCh38
NC_000023.10:g.69250351A>G , CM000685.1:g.69250351A>G	GRCh37
NC_000023.9:g.69167076A>G	NCBI36
NG_009809.1:g.419441A>G
NG_009809.2:g.419435A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.774A>G MANE Select	ENSP00000363680.4:p.Ser258=
ENST00000374552.8:c.774A>G	ENSP00000363680.4:p.Ser258=
ENST00000374553.6:c.774A>G	ENSP00000363681.2:p.Ser258=
ENST00000503592.5:c.378A>G	ENSP00000423037.1:p.Ser126=
ENST00000524573.5:c.774A>G	ENSP00000432585.1:p.Ser258=
ENST00000616899.1:c.378A>G	ENSP00000481963.1:p.Ser126=
NM_001005609.1:c.774A>G	NP_001005609.1:p.Ser258=
NM_001005612.2:c.774A>G	NP_001005612.2:p.Ser258=
NM_001399.4:c.774A>G	NP_001390.1:p.Ser258=
XM_006724630.2:c.774A>G	XP_006724693.1:p.Ser258=
XM_011530885.1:c.774A>G	XP_011529187.1:p.Ser258=
XM_011530885.2:c.774A>G	XP_011529187.1:p.Ser258=
XM_017029336.1:c.774A>G	XP_016884825.1:p.Ser258=
NM_001399.5:c.774A>G MANE Select	NP_001390.1:p.Ser258=
NM_001005609.2:c.774A>G	NP_001005609.1:p.Ser258=
NM_001005612.3:c.774A>G	NP_001005612.2:p.Ser258=