Canonical Allele Identifier: CA1429222208

Gene: CCDC50

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191375268A= , CM000665.2:g.191375268A=	GRCh38
NC_000003.11:g.191093057A= , CM000665.1:g.191093057A=	GRCh37
NC_000003.10:g.192575751A=	NCBI36
NG_008994.1:g.51184A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392455.9:c.655A= MANE Select	ENSP00000376249.4:p.Asn219=
ENST00000392456.4:c.449-4891A=	ENSP00000376250.4:n.449-4891A=
ENST00000392455.7:c.449-4891A=	ENSP00000376249.3:n.449-4891A=
ENST00000392456.3:c.655A=	ENSP00000376250.3:p.Asn219=
NM_174908.3:c.449-4891A=	NP_777568.1:n.449-4891A=
NM_178335.2:c.655A=	NP_848018.1:p.Asn219=
XM_011512460.1:c.655A=	XP_011510762.1:p.Asn219=
NM_178335.3:c.655A= MANE Select	NP_848018.1:p.Asn219=
NM_174908.4:c.449-4891A=	NP_777568.1:n.449-4891A=