Canonical Allele Identifier: CA2581890932

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191357223G>A , CM000665.2:g.191357223G>A	GRCh38
NC_000003.11:g.191075012G>A , CM000665.1:g.191075012G>A	GRCh37
NC_000003.10:g.192557706G>A	NCBI36
NG_008994.1:g.33139G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.112+73G>A MANE Select	ENSP00000376249.4:n.112+73G>A
ENST00000392456.4:c.112+73G>A	ENSP00000376250.4:n.112+73G>A
ENST00000392455.7:c.112+73G>A	ENSP00000376249.3:n.112+73G>A
ENST00000392456.3:c.112+73G>A	ENSP00000376250.3:n.112+73G>A
NM_174908.3:c.112+73G>A	NP_777568.1:n.112+73G>A
NM_178335.2:c.112+73G>A	NP_848018.1:n.112+73G>A
XM_011512460.1:c.112+73G>A	XP_011510762.1:n.112+73G>A
NM_178335.3:c.112+73G>A MANE Select	NP_848018.1:n.112+73G>A
NM_174908.4:c.112+73G>A	NP_777568.1:n.112+73G>A