Canonical Allele Identifier: CA1429201432

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191356935_191356936delinsTA , CM000665.2:g.191356935_191356936delinsTA	GRCh38
NC_000003.11:g.191074724_191074725delinsTA , CM000665.1:g.191074724_191074725delinsTA	GRCh37
NC_000003.10:g.192557418_192557419delinsTA	NCBI36
NG_008994.1:g.32851_32852delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.50-153_50-152delinsTA MANE Select	ENSP00000376249.4:n.50-153_50-152delinsTA
ENST00000392456.4:c.50-153_50-152delinsTA	ENSP00000376250.4:n.50-153_50-152delinsTA
ENST00000392455.7:c.50-153_50-152delinsTA	ENSP00000376249.3:n.50-153_50-152delinsTA
ENST00000392456.3:c.50-153_50-152delinsTA	ENSP00000376250.3:n.50-153_50-152delinsTA
NM_174908.3:c.50-153_50-152delinsTA	NP_777568.1:n.50-153_50-152delinsTA
NM_178335.2:c.50-153_50-152delinsTA	NP_848018.1:n.50-153_50-152delinsTA
XM_011512460.1:c.50-153_50-152delinsTA	XP_011510762.1:n.50-153_50-152delinsTA
NM_178335.3:c.50-153_50-152delinsTA MANE Select	NP_848018.1:n.50-153_50-152delinsTA
NM_174908.4:c.50-153_50-152delinsTA	NP_777568.1:n.50-153_50-152delinsTA