Canonical Allele Identifier: CA1429222185

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375233C= , CM000665.2:g.191375233C=	GRCh38
NC_000003.11:g.191093022C= , CM000665.1:g.191093022C=	GRCh37
NC_000003.10:g.192575716C=	NCBI36
NG_008994.1:g.51149C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.620C= MANE Select	ENSP00000376249.4:p.Ser207=
ENST00000392456.4:c.449-4926C=	ENSP00000376250.4:n.449-4926C=
ENST00000392455.7:c.449-4926C=	ENSP00000376249.3:n.449-4926C=
ENST00000392456.3:c.620C=	ENSP00000376250.3:p.Ser207=
NM_174908.3:c.449-4926C=	NP_777568.1:n.449-4926C=
NM_178335.2:c.620C=	NP_848018.1:p.Ser207=
XM_011512460.1:c.620C=	XP_011510762.1:p.Ser207=
NM_178335.3:c.620C= MANE Select	NP_848018.1:p.Ser207=
NM_174908.4:c.449-4926C=	NP_777568.1:n.449-4926C=