Canonical Allele Identifier: CA517007303

Gene: EDA

Linked Data

• MyVariant Identifiers: chrX:g.68836446T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.69616602T>C , CM000685.2:g.69616602T>C	GRCh38
NC_000023.10:g.68836446T>C , CM000685.1:g.68836446T>C	GRCh37
NC_000023.9:g.68753171T>C	NCBI36
NG_009809.1:g.5536T>C
NG_009809.2:g.5536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.294T>C MANE Select	ENSP00000363680.4:p.Pro98=
ENST00000338901.4:c.294T>C	ENSP00000340611.4:p.Pro98=
ENST00000374548.5:n.536T>C
ENST00000374552.8:c.294T>C	ENSP00000363680.4:p.Pro98=
ENST00000374553.6:c.294T>C	ENSP00000363681.2:p.Pro98=
ENST00000502251.5:n.536T>C
ENST00000524573.5:c.294T>C	ENSP00000432585.1:p.Pro98=
ENST00000525810.5:c.294T>C	ENSP00000434195.1:p.Pro98=
ENST00000527388.5:c.294T>C	ENSP00000434861.1:p.Pro98=
ENST00000533317.5:n.536T>C
NM_001005609.1:c.294T>C	NP_001005609.1:p.Pro98=
NM_001005610.3:c.294T>C	NP_001005610.2:p.Pro98=
NM_001005612.2:c.294T>C	NP_001005612.2:p.Pro98=
NM_001005613.3:c.294T>C	NP_001005613.1:p.Pro98=
NM_001399.4:c.294T>C	NP_001390.1:p.Pro98=
XM_006724630.2:c.294T>C	XP_006724693.1:p.Pro98=
XM_011530885.1:c.294T>C	XP_011529187.1:p.Pro98=
XM_011530885.2:c.294T>C	XP_011529187.1:p.Pro98=
XM_017029336.1:c.294T>C	XP_016884825.1:p.Pro98=
XM_017029337.1:c.294T>C	XP_016884826.1:p.Pro98=
XR_001755660.1:n.517T>C
NM_001399.5:c.294T>C MANE Select	NP_001390.1:p.Pro98=
NM_001005609.2:c.294T>C	NP_001005609.1:p.Pro98=
NM_001005610.4:c.294T>C	NP_001005610.2:p.Pro98=
NM_001005612.3:c.294T>C	NP_001005612.2:p.Pro98=
NM_001005613.4:c.294T>C	NP_001005613.1:p.Pro98=