Canonical Allele Identifier: CA1739107521
Gene: WNT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121334763C= , CM000669.2:g.121334763C= GRCh38
NC_000007.13:g.120974817C= , CM000669.1:g.120974817C= GRCh37
NC_000007.12:g.120762053C= NCBI36
NG_029242.1:g.14397C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222462.3:c.633+2799C= MANE Select ENSP00000222462.2:n.633+2799C=
ENST00000222462.2:c.633+2799C= ENSP00000222462.2:n.633+2799C=
ENST00000361301.6:c.603+2799C= ENSP00000355065.2:n.603+2799C=
NM_016087.2:c.603+2799C= NP_057171.2:n.603+2799C=
NM_057168.1:c.633+2799C= NP_476509.1:n.633+2799C=
NM_057168.2:c.633+2799C= MANE Select NP_476509.1:n.633+2799C=
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