Canonical Allele Identifier: CA2213436460

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641158_23641160delinsCGG , CM000678.2:g.23641158_23641160delinsCGG	GRCh38
NC_000016.9:g.23652479_23652481delinsCGG , CM000678.1:g.23652479_23652481delinsCGG	GRCh37
NC_000016.8:g.23559980_23559982delinsCGG	NCBI36
NG_007406.1:g.5198_5200delinsCCG , LRG_308:g.5198_5200delinsCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-855_-853delinsCCG	ENSP00000460666.3:n.-855_-853delinsCCG
ENST00000565038.2:c.-3_-1delinsCCG	ENSP00000459882.2:n.-3_-1delinsCCG
ENST00000566069.6:c.-3_-1delinsCCG	ENSP00000459237.2:n.-3_-1delinsCCG
ENST00000697377.2:c.-242_-240delinsCCG	ENSP00000513286.2:n.-242_-240delinsCCG
ENST00000697379.2:c.-148_-146delinsCCG	ENSP00000513287.2:n.-148_-146delinsCCG
ENST00000561514.2:c.-1746_-1744delinsCCG	ENSP00000460666.2:n.-1746_-1744delinsCCG
ENST00000697374.1:c.-1337_-1335delinsCCG	ENSP00000513284.1:n.-1337_-1335delinsCCG
ENST00000697376.1:c.-1058_-1056delinsCCG	ENSP00000513285.1:n.-1058_-1056delinsCCG
ENST00000697377.1:c.-1133_-1131delinsCCG	ENSP00000513286.1:n.-1133_-1131delinsCCG
ENST00000697379.1:c.-1039_-1037delinsCCG	ENSP00000513287.1:n.-1039_-1037delinsCCG
ENST00000697382.1:c.-1797_-1795delinsCCG	ENSP00000513288.1:n.-1797_-1795delinsCCG
ENST00000697383.1:c.-3_-1delinsCCG	ENSP00000513289.1:n.-3_-1delinsCCG
ENST00000697384.1:n.152_154delinsCCG
ENST00000261584.9:c.-3_-1delinsCCG MANE Select	ENSP00000261584.4:n.-3_-1delinsCCG
ENST00000261584.8:c.-3_-1delinsCCG	ENSP00000261584.4:n.-3_-1delinsCCG
ENST00000567003.1:n.142_144delinsCCG
ENST00000568219.5:c.-871_-869delinsCCG	ENSP00000454703.2:n.-871_-869delinsCCG
NM_024675.3:c.-3_-1delinsCCG , LRG_308t1:c.-3_-1delinsCCG	NP_078951.2:n.-3_-1delinsCCG
XM_011545948.1:c.-1022_-1020delinsCCG	XP_011544250.1:n.-1022_-1020delinsCCG
XM_011545946.2:c.-855_-853delinsCCG	XP_011544248.1:n.-855_-853delinsCCG
XM_011545947.2:c.-855_-853delinsCCG	XP_011544249.1:n.-855_-853delinsCCG
XM_011545948.2:c.-1022_-1020delinsCCG	XP_011544250.1:n.-1022_-1020delinsCCG
XM_017023671.1:c.-855_-853delinsCCG	XP_016879160.1:n.-855_-853delinsCCG
XM_017023672.2:c.-3_-1delinsCCG	XP_016879161.1:n.-3_-1delinsCCG
XM_017023673.2:c.-3_-1delinsCCG	XP_016879162.1:n.-3_-1delinsCCG
NM_024675.4:c.-3_-1delinsCCG MANE Select	NP_078951.2:n.-3_-1delinsCCG