Canonical Allele Identifier: CA1429222272

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375408G= , CM000665.2:g.191375408G=	GRCh38
NC_000003.11:g.191093197G= , CM000665.1:g.191093197G=	GRCh37
NC_000003.10:g.192575891G=	NCBI36
NG_008994.1:g.51324G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.795G= MANE Select	ENSP00000376249.4:p.Trp265=
ENST00000392456.4:c.449-4751G=	ENSP00000376250.4:n.449-4751G=
ENST00000392455.7:c.449-4751G=	ENSP00000376249.3:n.449-4751G=
ENST00000392456.3:c.795G=	ENSP00000376250.3:p.Trp265=
NM_174908.3:c.449-4751G=	NP_777568.1:n.449-4751G=
NM_178335.2:c.795G=	NP_848018.1:p.Trp265=
XM_011512460.1:c.795G=	XP_011510762.1:p.Trp265=
NM_178335.3:c.795G= MANE Select	NP_848018.1:p.Trp265=
NM_174908.4:c.449-4751G=	NP_777568.1:n.449-4751G=