Canonical Allele Identifier: CA2693980635

Gene: EDA

Linked Data

• gnomAD v4: X-70035272-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70035272G>A , CM000685.2:g.70035272G>A	GRCh38
NC_000023.10:g.69255122G>A , CM000685.1:g.69255122G>A	GRCh37
NC_000023.9:g.69171847G>A	NCBI36
NG_009809.1:g.424212G>A
NG_009809.2:g.424206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.925-86G>A MANE Select	ENSP00000363680.4:n.925-86G>A
ENST00000374552.8:c.925-86G>A	ENSP00000363680.4:n.925-86G>A
ENST00000374553.6:c.919-86G>A	ENSP00000363681.2:n.919-86G>A
ENST00000524573.5:c.910-86G>A	ENSP00000432585.1:n.910-86G>A
ENST00000616899.1:c.529-86G>A	ENSP00000481963.1:n.529-86G>A
NM_001005609.1:c.919-86G>A	NP_001005609.1:n.919-86G>A
NM_001005612.2:c.910-86G>A	NP_001005612.2:n.910-86G>A
NM_001399.4:c.925-86G>A	NP_001390.1:n.925-86G>A
XM_006724630.2:c.916-86G>A	XP_006724693.1:n.916-86G>A
XM_017029336.1:c.883-86G>A	XP_016884825.1:n.883-86G>A
NM_001399.5:c.925-86G>A MANE Select	NP_001390.1:n.925-86G>A
NM_001005609.2:c.919-86G>A	NP_001005609.1:n.919-86G>A
NM_001005612.3:c.910-86G>A	NP_001005612.2:n.910-86G>A