Canonical Allele Identifier: CA1429201472
Gene: CCDC50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191356993G= , CM000665.2:g.191356993G= GRCh38
NC_000003.11:g.191074782G= , CM000665.1:g.191074782G= GRCh37
NC_000003.10:g.192557476G= NCBI36
NG_008994.1:g.32909G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.50-95G= MANE Select ENSP00000376249.4:n.50-95G=
ENST00000392456.4:c.50-95G= ENSP00000376250.4:n.50-95G=
ENST00000392455.7:c.50-95G= ENSP00000376249.3:n.50-95G=
ENST00000392456.3:c.50-95G= ENSP00000376250.3:n.50-95G=
NM_174908.3:c.50-95G= NP_777568.1:n.50-95G=
NM_178335.2:c.50-95G= NP_848018.1:n.50-95G=
XM_011512460.1:c.50-95G= XP_011510762.1:n.50-95G=
NM_178335.3:c.50-95G= MANE Select NP_848018.1:n.50-95G=
NM_174908.4:c.50-95G= NP_777568.1:n.50-95G=