Canonical Allele Identifier: CA1429222127
Gene: CCDC50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375096T= , CM000665.2:g.191375096T= GRCh38
NC_000003.11:g.191092885T= , CM000665.1:g.191092885T= GRCh37
NC_000003.10:g.192575579T= NCBI36
NG_008994.1:g.51012T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.483T= MANE Select ENSP00000376249.4:p.Gly161=
ENST00000392456.4:c.448+5060T= ENSP00000376250.4:n.448+5060T=
ENST00000392455.7:c.448+5060T= ENSP00000376249.3:n.448+5060T=
ENST00000392456.3:c.483T= ENSP00000376250.3:p.Gly161=
NM_174908.3:c.448+5060T= NP_777568.1:n.448+5060T=
NM_178335.2:c.483T= NP_848018.1:p.Gly161=
XM_011512460.1:c.483T= XP_011510762.1:p.Gly161=
NM_178335.3:c.483T= MANE Select NP_848018.1:p.Gly161=
NM_174908.4:c.448+5060T= NP_777568.1:n.448+5060T=