Canonical Allele Identifier: CA355763822
Gene: CCDC50 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.191092928A>T (hg19) chr3:g.191375139A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375139A>T , CM000665.2:g.191375139A>T GRCh38
NC_000003.11:g.191092928A>T , CM000665.1:g.191092928A>T GRCh37
NC_000003.10:g.192575622A>T NCBI36
NG_008994.1:g.51055A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.526A>T MANE Select ENSP00000376249.4:p.Thr176Ser
ENST00000392456.4:c.449-5020A>T ENSP00000376250.4:n.449-5020A>T
ENST00000392455.7:c.449-5020A>T ENSP00000376249.3:n.449-5020A>T
ENST00000392456.3:c.526A>T ENSP00000376250.3:p.Thr176Ser
NM_174908.3:c.449-5020A>T NP_777568.1:n.449-5020A>T
NM_178335.2:c.526A>T NP_848018.1:p.Thr176Ser
XM_011512460.1:c.526A>T XP_011510762.1:p.Thr176Ser
NM_178335.3:c.526A>T MANE Select NP_848018.1:p.Thr176Ser
NM_174908.4:c.449-5020A>T NP_777568.1:n.449-5020A>T
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