Canonical Allele Identifier: CA1429222282

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375421C= , CM000665.2:g.191375421C=	GRCh38
NC_000003.11:g.191093210C= , CM000665.1:g.191093210C=	GRCh37
NC_000003.10:g.192575904C=	NCBI36
NG_008994.1:g.51337C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.808C= MANE Select	ENSP00000376249.4:p.Arg270=
ENST00000392456.4:c.449-4738C=	ENSP00000376250.4:n.449-4738C=
ENST00000392455.7:c.449-4738C=	ENSP00000376249.3:n.449-4738C=
ENST00000392456.3:c.808C=	ENSP00000376250.3:p.Arg270=
NM_174908.3:c.449-4738C=	NP_777568.1:n.449-4738C=
NM_178335.2:c.808C=	NP_848018.1:p.Arg270=
XM_011512460.1:c.808C=	XP_011510762.1:p.Arg270=
NM_178335.3:c.808C= MANE Select	NP_848018.1:p.Arg270=
NM_174908.4:c.449-4738C=	NP_777568.1:n.449-4738C=