Canonical Allele Identifier: CA182229442
Gene: CPQ HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.96784503C>A , CM000670.2:g.96784503C>A GRCh38
NC_000008.10:g.97796731C>A , CM000670.1:g.97796731C>A GRCh37
NC_000008.9:g.97865907C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220763.10:c.-34-361C>A MANE Select ENSP00000220763.5:n.-34-361C>A
ENST00000220763.9:c.-34-361C>A ENSP00000220763.5:n.-34-361C>A
ENST00000517742.1:c.-34-361C>A ENSP00000429146.1:n.-34-361C>A
ENST00000519484.1:c.-34-361C>A ENSP00000431114.1:n.-34-361C>A
ENST00000519900.1:c.-34-361C>A ENSP00000431024.1:n.-34-361C>A
ENST00000521142.1:c.-34-361C>A ENSP00000429934.1:n.-34-361C>A
ENST00000525310.1:n.104-361C>A
NM_016134.3:c.-34-361C>A NP_057218.1:n.-34-361C>A
XM_005250755.1:c.-34-361C>A XP_005250812.1:n.-34-361C>A
XM_006716498.2:c.-34-361C>A XP_006716561.1:n.-34-361C>A
XM_011516793.1:c.-34-361C>A XP_011515095.1:n.-34-361C>A
XM_011516794.1:c.-34-361C>A XP_011515096.1:n.-34-361C>A
XR_428374.1:n.177-361C>A
XR_928286.1:n.177-361C>A
XR_928433.1:n.354+7039G>T
NM_016134.4:c.-34-361C>A MANE Select NP_057218.1:n.-34-361C>A
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