Canonical Allele Identifier: CA1429222178
Gene: CCDC50 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375212C= , CM000665.2:g.191375212C= GRCh38
NC_000003.11:g.191093001C= , CM000665.1:g.191093001C= GRCh37
NC_000003.10:g.192575695C= NCBI36
NG_008994.1:g.51128C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.599C= MANE Select ENSP00000376249.4:p.Ser200=
ENST00000392456.4:c.449-4947C= ENSP00000376250.4:n.449-4947C=
ENST00000392455.7:c.449-4947C= ENSP00000376249.3:n.449-4947C=
ENST00000392456.3:c.599C= ENSP00000376250.3:p.Ser200=
NM_174908.3:c.449-4947C= NP_777568.1:n.449-4947C=
NM_178335.2:c.599C= NP_848018.1:p.Ser200=
XM_011512460.1:c.599C= XP_011510762.1:p.Ser200=
NM_178335.3:c.599C= MANE Select NP_848018.1:p.Ser200=
NM_174908.4:c.449-4947C= NP_777568.1:n.449-4947C=
Search 100 bp 5'
Search 100 bp 3'