Canonical Allele Identifier: CA413448340

Gene: EDA

Linked Data

• ClinVar Variation Id: 849399
• ClinVar RCV Id: RCV001053348
• dbSNP Id: rs2020138975
• MyVariant Identifiers: chrX:g.69247788C>T (hg19) ; chrX:g.70027938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027938C>T , CM000685.2:g.70027938C>T	GRCh38
NC_000023.10:g.69247788C>T , CM000685.1:g.69247788C>T	GRCh37
NC_000023.9:g.69164513C>T	NCBI36
NG_009809.1:g.416878C>T
NG_009809.2:g.416872C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.608C>T MANE Select	ENSP00000363680.4:p.Pro203Leu
ENST00000374552.8:c.608C>T	ENSP00000363680.4:p.Pro203Leu
ENST00000374553.6:c.608C>T	ENSP00000363681.2:p.Pro203Leu
ENST00000503592.5:c.212C>T	ENSP00000423037.1:p.Pro71Leu
ENST00000524573.5:c.608C>T	ENSP00000432585.1:p.Pro203Leu
ENST00000616899.1:c.212C>T	ENSP00000481963.1:p.Pro71Leu
NM_001005609.1:c.608C>T	NP_001005609.1:p.Pro203Leu
NM_001005612.2:c.608C>T	NP_001005612.2:p.Pro203Leu
NM_001399.4:c.608C>T	NP_001390.1:p.Pro203Leu
XM_006724630.2:c.608C>T	XP_006724693.1:p.Pro203Leu
XM_011530885.1:c.608C>T	XP_011529187.1:p.Pro203Leu
XM_011530885.2:c.608C>T	XP_011529187.1:p.Pro203Leu
XM_017029336.1:c.608C>T	XP_016884825.1:p.Pro203Leu
NM_001399.5:c.608C>T MANE Select	NP_001390.1:p.Pro203Leu
NM_001005609.2:c.608C>T	NP_001005609.1:p.Pro203Leu
NM_001005612.3:c.608C>T	NP_001005612.2:p.Pro203Leu