Canonical Allele Identifier: CA2213414517

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623981_23623988delinsAACAAATC , CM000678.2:g.23623981_23623988delinsAACAAATC	GRCh38
NC_000016.9:g.23635302_23635309delinsAACAAATC , CM000678.1:g.23635302_23635309delinsAACAAATC	GRCh37
NC_000016.8:g.23542803_23542810delinsAACAAATC	NCBI36
NG_007406.1:g.22370_22377delinsGATTTGTT , LRG_308:g.22370_22377delinsGATTTGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2840+21_2840+28delinsGATTTGTT	ENSP00000460666.3:n.2840+21_2840+28delinsGATTTGTT
ENST00000565038.2:c.*315+21_*315+28delinsGATTTGTT	ENSP00000459882.2:n.*315+21_*315+28delinsGATTTGTT
ENST00000566069.6:c.2834+21_2834+28delinsGATTTGTT	ENSP00000459237.2:n.2834+21_2834+28delinsGATTTGTT
ENST00000697377.2:c.2678+21_2678+28delinsGATTTGTT	ENSP00000513286.2:n.2678+21_2678+28delinsGATTTGTT
ENST00000697379.2:c.2840+21_2840+28delinsGATTTGTT	ENSP00000513287.2:n.2840+21_2840+28delinsGATTTGTT
ENST00000561514.2:c.1949+21_1949+28delinsGATTTGTT	ENSP00000460666.2:n.1949+21_1949+28delinsGATTTGTT
ENST00000697374.1:c.1949+21_1949+28delinsGATTTGTT	ENSP00000513284.1:n.1949+21_1949+28delinsGATTTGTT
ENST00000697375.1:n.4181+21_4181+28delinsGATTTGTT
ENST00000697376.1:c.1949+21_1949+28delinsGATTTGTT	ENSP00000513285.1:n.1949+21_1949+28delinsGATTTGTT
ENST00000697377.1:c.1787+21_1787+28delinsGATTTGTT	ENSP00000513286.1:n.1787+21_1787+28delinsGATTTGTT
ENST00000697378.1:n.3354+21_3354+28delinsGATTTGTT
ENST00000697379.1:c.1949+21_1949+28delinsGATTTGTT	ENSP00000513287.1:n.1949+21_1949+28delinsGATTTGTT
ENST00000697380.1:n.2126+21_2126+28delinsGATTTGTT
ENST00000697381.1:n.1529+21_1529+28delinsGATTTGTT
ENST00000697382.1:c.1949+21_1949+28delinsGATTTGTT	ENSP00000513288.1:n.1949+21_1949+28delinsGATTTGTT
ENST00000697383.1:c.368+21_368+28delinsGATTTGTT	ENSP00000513289.1:n.368+21_368+28delinsGATTTGTT
ENST00000261584.9:c.2834+21_2834+28delinsGATTTGTT MANE Select	ENSP00000261584.4:n.2834+21_2834+28delinsGATTTGTT
ENST00000261584.8:c.2834+21_2834+28delinsGATTTGTT	ENSP00000261584.4:n.2834+21_2834+28delinsGATTTGTT
ENST00000568219.5:c.1949+21_1949+28delinsGATTTGTT	ENSP00000454703.2:n.1949+21_1949+28delinsGATTTGTT
NM_024675.3:c.2834+21_2834+28delinsGATTTGTT , LRG_308t1:c.2834+21_2834+28delinsGATTTGTT	NP_078951.2:n.2834+21_2834+28delinsGATTTGTT
XM_011545946.1:c.2840+21_2840+28delinsGATTTGTT	XP_011544248.1:n.2840+21_2840+28delinsGATTTGTT
XM_011545947.1:c.2840+21_2840+28delinsGATTTGTT	XP_011544249.1:n.2840+21_2840+28delinsGATTTGTT
XM_011545948.1:c.1949+21_1949+28delinsGATTTGTT	XP_011544250.1:n.1949+21_1949+28delinsGATTTGTT
XR_950851.1:n.3630+21_3630+28delinsGATTTGTT
XM_011545946.2:c.2840+21_2840+28delinsGATTTGTT	XP_011544248.1:n.2840+21_2840+28delinsGATTTGTT
XM_011545947.2:c.2840+21_2840+28delinsGATTTGTT	XP_011544249.1:n.2840+21_2840+28delinsGATTTGTT
XM_011545948.2:c.1949+21_1949+28delinsGATTTGTT	XP_011544250.1:n.1949+21_1949+28delinsGATTTGTT
XM_017023671.1:c.2840+21_2840+28delinsGATTTGTT	XP_016879160.1:n.2840+21_2840+28delinsGATTTGTT
XM_017023672.2:c.2834+21_2834+28delinsGATTTGTT	XP_016879161.1:n.2834+21_2834+28delinsGATTTGTT
XM_017023673.2:c.2834+21_2834+28delinsGATTTGTT	XP_016879162.1:n.2834+21_2834+28delinsGATTTGTT
NM_024675.4:c.2834+21_2834+28delinsGATTTGTT MANE Select	NP_078951.2:n.2834+21_2834+28delinsGATTTGTT