Canonical Allele Identifier: CA2061868417
Gene: WSCD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250227_108250229delinsGAC , CM000674.2:g.108250227_108250229delinsGAC GRCh38
NC_000012.11:g.108644004_108644006delinsGAC , CM000674.1:g.108644004_108644006delinsGAC GRCh37
NC_000012.10:g.107168134_107168136delinsGAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000547525.6:c.*1884_*1886delinsGAC MANE Select ENSP00000448047.1:n.*1884_*1886delinsGAC
ENST00000332082.8:c.*1884_*1886delinsGAC ENSP00000331933.4:n.*1884_*1886delinsGAC
NM_001304447.1:c.*1884_*1886delinsGAC NP_001291376.1:n.*1884_*1886delinsGAC
NM_014653.3:c.*1884_*1886delinsGAC NP_055468.2:n.*1884_*1886delinsGAC
NM_014653.4:c.*1884_*1886delinsGAC MANE Select NP_055468.2:n.*1884_*1886delinsGAC
NM_001304447.2:c.*1884_*1886delinsGAC NP_001291376.1:n.*1884_*1886delinsGAC
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