Canonical Allele Identifier: CA517013919

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.69253279T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033429T>G , CM000685.2:g.70033429T>G	GRCh38
NC_000023.10:g.69253279T>G , CM000685.1:g.69253279T>G	GRCh37
NC_000023.9:g.69170004T>G	NCBI36
NG_009809.1:g.422369T>G
NG_009809.2:g.422363T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.825T>G MANE Select	ENSP00000363680.4:p.Ser275=
ENST00000374552.8:c.825T>G	ENSP00000363680.4:p.Ser275=
ENST00000374553.6:c.825T>G	ENSP00000363681.2:p.Ser275=
ENST00000524573.5:c.816T>G	ENSP00000432585.1:p.Ser272=
ENST00000616899.1:c.429T>G	ENSP00000481963.1:p.Ser143=
NM_001005609.1:c.825T>G	NP_001005609.1:p.Ser275=
NM_001005612.2:c.816T>G	NP_001005612.2:p.Ser272=
NM_001399.4:c.825T>G	NP_001390.1:p.Ser275=
XM_006724630.2:c.816T>G	XP_006724693.1:p.Ser272=
XM_011530885.1:c.825T>G	XP_011529187.1:p.Ser275=
XM_011530885.2:c.825T>G	XP_011529187.1:p.Ser275=
XM_017029336.1:c.825T>G	XP_016884825.1:p.Ser275=
NM_001399.5:c.825T>G MANE Select	NP_001390.1:p.Ser275=
NM_001005609.2:c.825T>G	NP_001005609.1:p.Ser275=
NM_001005612.3:c.816T>G	NP_001005612.2:p.Ser272=