Canonical Allele Identifier: CA2435979513

Gene: EDA

Linked Data

• dbSNP Id: rs2020132683
• gnomAD v4: X-70027804-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70027805dup , CM000685.2:g.70027805dup	GRCh38
NC_000023.10:g.69247655dup , CM000685.1:g.69247655dup	GRCh37
NC_000023.9:g.69164380dup	NCBI36
NG_009809.1:g.416745dup
NG_009809.2:g.416739dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.527-52dup MANE Select	ENSP00000363680.4:n.527-52dup
ENST00000374552.8:c.527-52dup	ENSP00000363680.4:n.527-52dup
ENST00000374553.6:c.527-52dup	ENSP00000363681.2:n.527-52dup
ENST00000503592.5:c.131-52dup	ENSP00000423037.1:n.131-52dup
ENST00000524573.5:c.527-52dup	ENSP00000432585.1:n.527-52dup
ENST00000616899.1:c.131-52dup	ENSP00000481963.1:n.131-52dup
NM_001005609.1:c.527-52dup	NP_001005609.1:n.527-52dup
NM_001005612.2:c.527-52dup	NP_001005612.2:n.527-52dup
NM_001399.4:c.527-52dup	NP_001390.1:n.527-52dup
XM_006724630.2:c.527-52dup	XP_006724693.1:n.527-52dup
XM_011530885.1:c.527-52dup	XP_011529187.1:n.527-52dup
XM_011530885.2:c.527-52dup	XP_011529187.1:n.527-52dup
XM_017029336.1:c.527-52dup	XP_016884825.1:n.527-52dup
NM_001399.5:c.527-52dup MANE Select	NP_001390.1:n.527-52dup
NM_001005609.2:c.527-52dup	NP_001005609.1:n.527-52dup
NM_001005612.3:c.527-52dup	NP_001005612.2:n.527-52dup