Canonical Allele Identifier: CA517013941

Gene: EDA

Linked Data

• ClinVar Variation Id: 2871008
• ClinVar RCV Id: RCV003638242
• MyVariant Identifiers: chrX:g.69253285C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033435C>T , CM000685.2:g.70033435C>T	GRCh38
NC_000023.10:g.69253285C>T , CM000685.1:g.69253285C>T	GRCh37
NC_000023.9:g.69170010C>T	NCBI36
NG_009809.1:g.422375C>T
NG_009809.2:g.422369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.831C>T MANE Select	ENSP00000363680.4:p.Ile277=
ENST00000374552.8:c.831C>T	ENSP00000363680.4:p.Ile277=
ENST00000374553.6:c.831C>T	ENSP00000363681.2:p.Ile277=
ENST00000524573.5:c.822C>T	ENSP00000432585.1:p.Ile274=
ENST00000616899.1:c.435C>T	ENSP00000481963.1:p.Ile145=
NM_001005609.1:c.831C>T	NP_001005609.1:p.Ile277=
NM_001005612.2:c.822C>T	NP_001005612.2:p.Ile274=
NM_001399.4:c.831C>T	NP_001390.1:p.Ile277=
XM_006724630.2:c.822C>T	XP_006724693.1:p.Ile274=
XM_011530885.1:c.831C>T	XP_011529187.1:p.Ile277=
XM_011530885.2:c.831C>T	XP_011529187.1:p.Ile277=
XM_017029336.1:c.831C>T	XP_016884825.1:p.Ile277=
NM_001399.5:c.831C>T MANE Select	NP_001390.1:p.Ile277=
NM_001005609.2:c.831C>T	NP_001005609.1:p.Ile277=
NM_001005612.3:c.822C>T	NP_001005612.2:p.Ile274=