Canonical Allele Identifier: CA1804688127

Gene: CPQ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97142213A= , CM000670.2:g.97142213A=	GRCh38
NC_000008.10:g.98154441A= , CM000670.1:g.98154441A=	GRCh37
NC_000008.9:g.98223617A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220763.10:c.1256-807A= MANE Select	ENSP00000220763.5:n.1256-807A=
ENST00000220763.9:c.1256-807A=	ENSP00000220763.5:n.1256-807A=
ENST00000522617.3:c.229-807A=
NM_016134.3:c.1256-807A=	NP_057218.1:n.1256-807A=
NR_125390.1:n.472-188603T=
XM_005250755.1:c.1256-807A=	XP_005250812.1:n.1256-807A=
XM_011516793.1:c.1256-807A=	XP_011515095.1:n.1256-807A=
XM_011516794.1:c.1256-807A=	XP_011515096.1:n.1256-807A=
XR_428374.1:n.1533-807A=
XR_928286.1:n.1583-807A=
NM_016134.4:c.1256-807A= MANE Select	NP_057218.1:n.1256-807A=