Canonical Allele Identifier: CA2669071422

Gene: CCDC50

Linked Data

• gnomAD v4: 3-191356937-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191356938dup , CM000665.2:g.191356938dup	GRCh38
NC_000003.11:g.191074727dup , CM000665.1:g.191074727dup	GRCh37
NC_000003.10:g.192557421dup	NCBI36
NG_008994.1:g.32854dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.50-150dup MANE Select	ENSP00000376249.4:n.50-150dup
ENST00000392456.4:c.50-150dup	ENSP00000376250.4:n.50-150dup
ENST00000392455.7:c.50-150dup	ENSP00000376249.3:n.50-150dup
ENST00000392456.3:c.50-150dup	ENSP00000376250.3:n.50-150dup
NM_174908.3:c.50-150dup	NP_777568.1:n.50-150dup
NM_178335.2:c.50-150dup	NP_848018.1:n.50-150dup
XM_011512460.1:c.50-150dup	XP_011510762.1:n.50-150dup
NM_178335.3:c.50-150dup MANE Select	NP_848018.1:n.50-150dup
NM_174908.4:c.50-150dup	NP_777568.1:n.50-150dup