Canonical Allele Identifier: CA2209586011

Gene: PDXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15056976A= , CM000678.2:g.15056976A=	GRCh38
NC_000016.9:g.15150833A= , CM000678.1:g.15150833A=	GRCh37
NC_000016.8:g.15058334A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001285449.1:c.1399+26920A=	NP_001272378.1:n.1399+26920A=
NM_001285449.2:c.1399+26920A=	NP_001272378.1:n.1399+26920A=
NM_001324020.1:c.1396+26920A=	NP_001310949.1:n.1396+26920A=
NM_001324020.2:c.1396+26920A=	NP_001310949.1:n.1396+26920A=
NM_001324021.1:c.1318+26920A=	NP_001310950.1:n.1318+26920A=
NM_001324021.2:c.1318+26920A=	NP_001310950.1:n.1318+26920A=
ENST00000535621.6:c.1399+26920A=	ENSP00000437835.2:n.1399+26920A=
XM_017023065.1:c.1354+26920A=	XP_016878554.1:n.1354+26920A=
XM_024450194.1:c.1354+26920A=	XP_024305962.1:n.1354+26920A=
XM_024450195.1:c.1453+26920A=	XP_024305963.1:n.1453+26920A=
XM_024450196.1:c.1426+26920A=	XP_024305964.1:n.1426+26920A=
XM_024450197.1:c.1273+26920A=	XP_024305965.1:n.1273+26920A=