Canonical Allele Identifier: CA1804688238
Gene: CPQ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97142321T= , CM000670.2:g.97142321T= GRCh38
NC_000008.10:g.98154549T= , CM000670.1:g.98154549T= GRCh37
NC_000008.9:g.98223725T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220763.10:c.1256-699T= MANE Select ENSP00000220763.5:n.1256-699T=
ENST00000220763.9:c.1256-699T= ENSP00000220763.5:n.1256-699T=
ENST00000522617.3:c.229-699T=
NM_016134.3:c.1256-699T= NP_057218.1:n.1256-699T=
NR_125390.1:n.472-188711A=
XM_005250755.1:c.1256-699T= XP_005250812.1:n.1256-699T=
XM_011516793.1:c.1256-699T= XP_011515095.1:n.1256-699T=
XM_011516794.1:c.1256-699T= XP_011515096.1:n.1256-699T=
XR_428374.1:n.1533-699T=
XR_928286.1:n.1583-699T=
NM_016134.4:c.1256-699T= MANE Select NP_057218.1:n.1256-699T=
Search 100 bp 5'
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