Canonical Allele Identifier: CA1804688147

Gene: CPQ

Linked Data

• dbSNP Id: rs1812180824

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97142240A>C , CM000670.2:g.97142240A>C	GRCh38
NC_000008.10:g.98154468A>C , CM000670.1:g.98154468A>C	GRCh37
NC_000008.9:g.98223644A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000220763.10:c.1256-780A>C MANE Select	ENSP00000220763.5:n.1256-780A>C
ENST00000220763.9:c.1256-780A>C	ENSP00000220763.5:n.1256-780A>C
ENST00000522617.3:c.229-780A>C
NM_016134.3:c.1256-780A>C	NP_057218.1:n.1256-780A>C
NR_125390.1:n.472-188630T>G
XM_005250755.1:c.1256-780A>C	XP_005250812.1:n.1256-780A>C
XM_011516793.1:c.1256-780A>C	XP_011515095.1:n.1256-780A>C
XM_011516794.1:c.1256-780A>C	XP_011515096.1:n.1256-780A>C
XR_428374.1:n.1533-780A>C
XR_928286.1:n.1583-780A>C
NM_016134.4:c.1256-780A>C MANE Select	NP_057218.1:n.1256-780A>C