Canonical Allele Identifier: CA517012663

Gene: EDA

Linked Data

• gnomAD v4: X-70027882-C-T
• MyVariant Identifiers: chrX:g.69247732C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027882C>T , CM000685.2:g.70027882C>T	GRCh38
NC_000023.10:g.69247732C>T , CM000685.1:g.69247732C>T	GRCh37
NC_000023.9:g.69164457C>T	NCBI36
NG_009809.1:g.416822C>T
NG_009809.2:g.416816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.552C>T MANE Select	ENSP00000363680.4:p.Pro184=
ENST00000374552.8:c.552C>T	ENSP00000363680.4:p.Pro184=
ENST00000374553.6:c.552C>T	ENSP00000363681.2:p.Pro184=
ENST00000503592.5:c.156C>T	ENSP00000423037.1:p.Pro52=
ENST00000524573.5:c.552C>T	ENSP00000432585.1:p.Pro184=
ENST00000616899.1:c.156C>T	ENSP00000481963.1:p.Pro52=
NM_001005609.1:c.552C>T	NP_001005609.1:p.Pro184=
NM_001005612.2:c.552C>T	NP_001005612.2:p.Pro184=
NM_001399.4:c.552C>T	NP_001390.1:p.Pro184=
XM_006724630.2:c.552C>T	XP_006724693.1:p.Pro184=
XM_011530885.1:c.552C>T	XP_011529187.1:p.Pro184=
XM_011530885.2:c.552C>T	XP_011529187.1:p.Pro184=
XM_017029336.1:c.552C>T	XP_016884825.1:p.Pro184=
NM_001399.5:c.552C>T MANE Select	NP_001390.1:p.Pro184=
NM_001005609.2:c.552C>T	NP_001005609.1:p.Pro184=
NM_001005612.3:c.552C>T	NP_001005612.2:p.Pro184=