Canonical Allele Identifier: CA1804688140

Gene: CPQ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97142234G= , CM000670.2:g.97142234G=	GRCh38
NC_000008.10:g.98154462G= , CM000670.1:g.98154462G=	GRCh37
NC_000008.9:g.98223638G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000220763.10:c.1256-786G= MANE Select	ENSP00000220763.5:n.1256-786G=
ENST00000220763.9:c.1256-786G=	ENSP00000220763.5:n.1256-786G=
ENST00000522617.3:c.229-786G=
NM_016134.3:c.1256-786G=	NP_057218.1:n.1256-786G=
NR_125390.1:n.472-188624C=
XM_005250755.1:c.1256-786G=	XP_005250812.1:n.1256-786G=
XM_011516793.1:c.1256-786G=	XP_011515095.1:n.1256-786G=
XM_011516794.1:c.1256-786G=	XP_011515096.1:n.1256-786G=
XR_428374.1:n.1533-786G=
XR_928286.1:n.1583-786G=
NM_016134.4:c.1256-786G= MANE Select	NP_057218.1:n.1256-786G=