Canonical Allele Identifier: CA2531774938

Gene: CPQ

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97142279G>A , CM000670.2:g.97142279G>A	GRCh38
NC_000008.10:g.98154507G>A , CM000670.1:g.98154507G>A	GRCh37
NC_000008.9:g.98223683G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220763.10:c.1256-741G>A MANE Select	ENSP00000220763.5:n.1256-741G>A
ENST00000220763.9:c.1256-741G>A	ENSP00000220763.5:n.1256-741G>A
ENST00000522617.3:c.229-741G>A
NM_016134.3:c.1256-741G>A	NP_057218.1:n.1256-741G>A
NR_125390.1:n.472-188669C>T
XM_005250755.1:c.1256-741G>A	XP_005250812.1:n.1256-741G>A
XM_011516793.1:c.1256-741G>A	XP_011515095.1:n.1256-741G>A
XM_011516794.1:c.1256-741G>A	XP_011515096.1:n.1256-741G>A
XR_428374.1:n.1533-741G>A
XR_928286.1:n.1583-741G>A
NM_016134.4:c.1256-741G>A MANE Select	NP_057218.1:n.1256-741G>A