Canonical Allele Identifier: CA413449009

Gene: EDA

Linked Data

• gnomAD v4: X-70033511-A-C
• MyVariant Identifiers: chrX:g.69253361A>C (hg19) ; chrX:g.70033511A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033511A>C , CM000685.2:g.70033511A>C	GRCh38
NC_000023.10:g.69253361A>C , CM000685.1:g.69253361A>C	GRCh37
NC_000023.9:g.69170086A>C	NCBI36
NG_009809.1:g.422451A>C
NG_009809.2:g.422445A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374552.9:c.907A>C MANE Select	ENSP00000363680.4:p.Ile303Leu
ENST00000374552.8:c.907A>C	ENSP00000363680.4:p.Ile303Leu
ENST00000374553.6:c.907A>C	ENSP00000363681.2:p.Ile303Leu
ENST00000524573.5:c.898A>C	ENSP00000432585.1:p.Ile300Leu
ENST00000616899.1:c.511A>C	ENSP00000481963.1:p.Ile171Leu
NM_001005609.1:c.907A>C	NP_001005609.1:p.Ile303Leu
NM_001005612.2:c.898A>C	NP_001005612.2:p.Ile300Leu
NM_001399.4:c.907A>C	NP_001390.1:p.Ile303Leu
XM_006724630.2:c.898A>C	XP_006724693.1:p.Ile300Leu
XM_011530885.1:c.907A>C	XP_011529187.1:p.Ile303Leu
XM_011530885.2:c.907A>C	XP_011529187.1:p.Ile303Leu
XM_017029336.1:c.882+25A>C	XP_016884825.1:n.882+25A>C
NM_001399.5:c.907A>C MANE Select	NP_001390.1:p.Ile303Leu
NM_001005609.2:c.907A>C	NP_001005609.1:p.Ile303Leu
NM_001005612.3:c.898A>C	NP_001005612.2:p.Ile300Leu