Canonical Allele Identifier: CA2693980269

Gene: EDA

Linked Data

• gnomAD v4: X-70033543-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70033545del , CM000685.2:g.70033545del	GRCh38
NC_000023.10:g.69253395del , CM000685.1:g.69253395del	GRCh37
NC_000023.9:g.69170120del	NCBI36
NG_009809.1:g.422485del
NG_009809.2:g.422479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374552.9:c.924+17del MANE Select	ENSP00000363680.4:n.924+17del
ENST00000374552.8:c.924+17del	ENSP00000363680.4:n.924+17del
ENST00000374553.6:c.918+23del	ENSP00000363681.2:n.918+23del
ENST00000524573.5:c.909+23del	ENSP00000432585.1:n.909+23del
ENST00000616899.1:c.528+17del	ENSP00000481963.1:n.528+17del
NM_001005609.1:c.918+23del	NP_001005609.1:n.918+23del
NM_001005612.2:c.909+23del	NP_001005612.2:n.909+23del
NM_001399.4:c.924+17del	NP_001390.1:n.924+17del
XM_006724630.2:c.915+17del	XP_006724693.1:n.915+17del
XM_011530885.1:c.918+23del	XP_011529187.1:n.918+23del
XM_011530885.2:c.918+23del	XP_011529187.1:n.918+23del
XM_017029336.1:c.882+59del	XP_016884825.1:n.882+59del
NM_001399.5:c.924+17del MANE Select	NP_001390.1:n.924+17del
NM_001005609.2:c.918+23del	NP_001005609.1:n.918+23del
NM_001005612.3:c.909+23del	NP_001005612.2:n.909+23del