Canonical Allele Identifier: CA1429222369

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375603G= , CM000665.2:g.191375603G=	GRCh38
NC_000003.11:g.191093392G= , CM000665.1:g.191093392G=	GRCh37
NC_000003.10:g.192576086G=	NCBI36
NG_008994.1:g.51519G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000392455.9:c.976+14G= MANE Select	ENSP00000376249.4:n.976+14G=
ENST00000392456.4:c.449-4556G=	ENSP00000376250.4:n.449-4556G=
ENST00000392455.7:c.449-4556G=	ENSP00000376249.3:n.449-4556G=
ENST00000392456.3:c.976+14G=	ENSP00000376250.3:n.976+14G=
NM_174908.3:c.449-4556G=	NP_777568.1:n.449-4556G=
NM_178335.2:c.976+14G=	NP_848018.1:n.976+14G=
XM_011512460.1:c.976+14G=	XP_011510762.1:n.976+14G=
NM_178335.3:c.976+14G= MANE Select	NP_848018.1:n.976+14G=
NM_174908.4:c.449-4556G=	NP_777568.1:n.449-4556G=