Canonical Allele Identifier: CA1429201830
Gene: CCDC50 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191357183T= , CM000665.2:g.191357183T= GRCh38
NC_000003.11:g.191074972T= , CM000665.1:g.191074972T= GRCh37
NC_000003.10:g.192557666T= NCBI36
NG_008994.1:g.33099T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392455.9:c.112+33T= MANE Select ENSP00000376249.4:n.112+33T=
ENST00000392456.4:c.112+33T= ENSP00000376250.4:n.112+33T=
ENST00000392455.7:c.112+33T= ENSP00000376249.3:n.112+33T=
ENST00000392456.3:c.112+33T= ENSP00000376250.3:n.112+33T=
NM_174908.3:c.112+33T= NP_777568.1:n.112+33T=
NM_178335.2:c.112+33T= NP_848018.1:n.112+33T=
XM_011512460.1:c.112+33T= XP_011510762.1:n.112+33T=
NM_178335.3:c.112+33T= MANE Select NP_848018.1:n.112+33T=
NM_174908.4:c.112+33T= NP_777568.1:n.112+33T=
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