Canonical Allele Identifier: CA2620705718
Gene: WSCD2 HGNC NCBI

Linked Data

gnomAD v4: 12-108250201-T-TGAGAGA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250214_108250219dup , CM000674.2:g.108250214_108250219dup GRCh38
NC_000012.11:g.108643991_108643996dup , CM000674.1:g.108643991_108643996dup GRCh37
NC_000012.10:g.107168121_107168126dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000547525.6:c.*1871_*1876dup MANE Select ENSP00000448047.1:n.*1871_*1876dup
ENST00000332082.8:c.*1871_*1876dup ENSP00000331933.4:n.*1871_*1876dup
NM_001304447.1:c.*1871_*1876dup NP_001291376.1:n.*1871_*1876dup
NM_014653.3:c.*1871_*1876dup NP_055468.2:n.*1871_*1876dup
NM_014653.4:c.*1871_*1876dup MANE Select NP_055468.2:n.*1871_*1876dup
NM_001304447.2:c.*1871_*1876dup NP_001291376.1:n.*1871_*1876dup
Search 100 bp 5'
Search 100 bp 3'