Canonical Allele Identifier: CA1429201836
Gene: CCDC50 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191357192T= , CM000665.2:g.191357192T= GRCh38
NC_000003.11:g.191074981T= , CM000665.1:g.191074981T= GRCh37
NC_000003.10:g.192557675T= NCBI36
NG_008994.1:g.33108T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.112+42T= MANE Select ENSP00000376249.4:n.112+42T=
ENST00000392456.4:c.112+42T= ENSP00000376250.4:n.112+42T=
ENST00000392455.7:c.112+42T= ENSP00000376249.3:n.112+42T=
ENST00000392456.3:c.112+42T= ENSP00000376250.3:n.112+42T=
NM_174908.3:c.112+42T= NP_777568.1:n.112+42T=
NM_178335.2:c.112+42T= NP_848018.1:n.112+42T=
XM_011512460.1:c.112+42T= XP_011510762.1:n.112+42T=
NM_178335.3:c.112+42T= MANE Select NP_848018.1:n.112+42T=
NM_174908.4:c.112+42T= NP_777568.1:n.112+42T=
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