Canonical Allele Identifier: CA1429201672
Gene: CCDC50 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191357083T= , CM000665.2:g.191357083T= GRCh38
NC_000003.11:g.191074872T= , CM000665.1:g.191074872T= GRCh37
NC_000003.10:g.192557566T= NCBI36
NG_008994.1:g.32999T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.50-5T= MANE Select ENSP00000376249.4:n.50-5T=
ENST00000392456.4:c.50-5T= ENSP00000376250.4:n.50-5T=
ENST00000392455.7:c.50-5T= ENSP00000376249.3:n.50-5T=
ENST00000392456.3:c.50-5T= ENSP00000376250.3:n.50-5T=
NM_174908.3:c.50-5T= NP_777568.1:n.50-5T=
NM_178335.2:c.50-5T= NP_848018.1:n.50-5T=
XM_011512460.1:c.50-5T= XP_011510762.1:n.50-5T=
NM_178335.3:c.50-5T= MANE Select NP_848018.1:n.50-5T=
NM_174908.4:c.50-5T= NP_777568.1:n.50-5T=
Search 100 bp 5'
Search 100 bp 3'