Canonical Allele Identifier: CA2061868413
Gene: WSCD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108250224A= , CM000674.2:g.108250224A= GRCh38
NC_000012.11:g.108644001A= , CM000674.1:g.108644001A= GRCh37
NC_000012.10:g.107168131A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000547525.6:c.*1881A= MANE Select ENSP00000448047.1:n.*1881A=
ENST00000332082.8:c.*1881A= ENSP00000331933.4:n.*1881A=
NM_001304447.1:c.*1881A= NP_001291376.1:n.*1881A=
NM_014653.3:c.*1881A= NP_055468.2:n.*1881A=
NM_014653.4:c.*1881A= MANE Select NP_055468.2:n.*1881A=
NM_001304447.2:c.*1881A= NP_001291376.1:n.*1881A=
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