Canonical Allele Identifier: CA1429222139
Gene: CCDC50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375129A= , CM000665.2:g.191375129A= GRCh38
NC_000003.11:g.191092918A= , CM000665.1:g.191092918A= GRCh37
NC_000003.10:g.192575612A= NCBI36
NG_008994.1:g.51045A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.516A= MANE Select ENSP00000376249.4:p.Arg172=
ENST00000392456.4:c.449-5030A= ENSP00000376250.4:n.449-5030A=
ENST00000392455.7:c.449-5030A= ENSP00000376249.3:n.449-5030A=
ENST00000392456.3:c.516A= ENSP00000376250.3:p.Arg172=
NM_174908.3:c.449-5030A= NP_777568.1:n.449-5030A=
NM_178335.2:c.516A= NP_848018.1:p.Arg172=
XM_011512460.1:c.516A= XP_011510762.1:p.Arg172=
NM_178335.3:c.516A= MANE Select NP_848018.1:p.Arg172=
NM_174908.4:c.449-5030A= NP_777568.1:n.449-5030A=