Canonical Allele Identifier: CA2620705735

Gene: WSCD2

Linked Data

• gnomAD v4: 12-108250218-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108250219del , CM000674.2:g.108250219del	GRCh38
NC_000012.11:g.108643996del , CM000674.1:g.108643996del	GRCh37
NC_000012.10:g.107168126del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547525.6:c.*1876del MANE Select	ENSP00000448047.1:n.*1876del
ENST00000332082.8:c.*1876del	ENSP00000331933.4:n.*1876del
NM_001304447.1:c.*1876del	NP_001291376.1:n.*1876del
NM_014653.3:c.*1876del	NP_055468.2:n.*1876del
NM_014653.4:c.*1876del MANE Select	NP_055468.2:n.*1876del
NM_001304447.2:c.*1876del	NP_001291376.1:n.*1876del