Canonical Allele Identifier: CA1429222367
Gene: CCDC50 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.191375601C= , CM000665.2:g.191375601C= GRCh38
NC_000003.11:g.191093390C= , CM000665.1:g.191093390C= GRCh37
NC_000003.10:g.192576084C= NCBI36
NG_008994.1:g.51517C=

Transcript Alleles

HGVS Amino-acid change
ENST00000392455.9:c.976+12C= MANE Select ENSP00000376249.4:n.976+12C=
ENST00000392456.4:c.449-4558C= ENSP00000376250.4:n.449-4558C=
ENST00000392455.7:c.449-4558C= ENSP00000376249.3:n.449-4558C=
ENST00000392456.3:c.976+12C= ENSP00000376250.3:n.976+12C=
NM_174908.3:c.449-4558C= NP_777568.1:n.449-4558C=
NM_178335.2:c.976+12C= NP_848018.1:n.976+12C=
XM_011512460.1:c.976+12C= XP_011510762.1:n.976+12C=
NM_178335.3:c.976+12C= MANE Select NP_848018.1:n.976+12C=
NM_174908.4:c.449-4558C= NP_777568.1:n.449-4558C=