Canonical Allele Identifier: CA2061868407
Gene: WSCD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250220C= , CM000674.2:g.108250220C= GRCh38
NC_000012.11:g.108643997C= , CM000674.1:g.108643997C= GRCh37
NC_000012.10:g.107168127C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000547525.6:c.*1877C= MANE Select ENSP00000448047.1:n.*1877C=
ENST00000332082.8:c.*1877C= ENSP00000331933.4:n.*1877C=
NM_001304447.1:c.*1877C= NP_001291376.1:n.*1877C=
NM_014653.3:c.*1877C= NP_055468.2:n.*1877C=
NM_014653.4:c.*1877C= MANE Select NP_055468.2:n.*1877C=
NM_001304447.2:c.*1877C= NP_001291376.1:n.*1877C=
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