Canonical Allele Identifier: CA2213436411

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641108_23641109delinsAC , CM000678.2:g.23641108_23641109delinsAC	GRCh38
NC_000016.9:g.23652429_23652430delinsAC , CM000678.1:g.23652429_23652430delinsAC	GRCh37
NC_000016.8:g.23559930_23559931delinsAC	NCBI36
NG_007406.1:g.5249_5250delinsGT , LRG_308:g.5249_5250delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-804_-803delinsGT	ENSP00000460666.3:n.-804_-803delinsGT
ENST00000565038.2:c.48+1_48+2delinsGT	ENSP00000459882.2:n.48+1_48+2delinsGT
ENST00000566069.6:c.48+1_48+2delinsGT	ENSP00000459237.2:n.48+1_48+2delinsGT
ENST00000697377.2:c.-192+1_-192+2delinsGT	ENSP00000513286.2:n.-192+1_-192+2delinsGT
ENST00000697379.2:c.-98+1_-98+2delinsGT	ENSP00000513287.2:n.-98+1_-98+2delinsGT
ENST00000561514.2:c.-1695_-1694delinsGT	ENSP00000460666.2:n.-1695_-1694delinsGT
ENST00000697374.1:c.-1286_-1285delinsGT	ENSP00000513284.1:n.-1286_-1285delinsGT
ENST00000697376.1:c.-1008+1_-1008+2delinsGT	ENSP00000513285.1:n.-1008+1_-1008+2delinsGT
ENST00000697377.1:c.-1083+1_-1083+2delinsGT	ENSP00000513286.1:n.-1083+1_-1083+2delinsGT
ENST00000697379.1:c.-989+1_-989+2delinsGT	ENSP00000513287.1:n.-989+1_-989+2delinsGT
ENST00000697382.1:c.-1746_-1745delinsGT	ENSP00000513288.1:n.-1746_-1745delinsGT
ENST00000697383.1:c.48+1_48+2delinsGT	ENSP00000513289.1:n.48+1_48+2delinsGT
ENST00000697384.1:n.202+1_202+2delinsGT
ENST00000261584.9:c.48+1_48+2delinsGT MANE Select	ENSP00000261584.4:n.48+1_48+2delinsGT
ENST00000261584.8:c.48+1_48+2delinsGT	ENSP00000261584.4:n.48+1_48+2delinsGT
ENST00000567003.1:n.192+1_192+2delinsGT
ENST00000568219.5:c.-838+18_-838+19delinsGT	ENSP00000454703.2:n.-838+18_-838+19delinsGT
NM_024675.3:c.48+1_48+2delinsGT , LRG_308t1:c.48+1_48+2delinsGT	NP_078951.2:n.48+1_48+2delinsGT
XM_011545948.1:c.-972+1_-972+2delinsGT	XP_011544250.1:n.-972+1_-972+2delinsGT
XM_011545946.2:c.-804_-803delinsGT	XP_011544248.1:n.-804_-803delinsGT
XM_011545947.2:c.-804_-803delinsGT	XP_011544249.1:n.-804_-803delinsGT
XM_011545948.2:c.-972+1_-972+2delinsGT	XP_011544250.1:n.-972+1_-972+2delinsGT
XM_017023671.1:c.-804_-803delinsGT	XP_016879160.1:n.-804_-803delinsGT
XM_017023672.2:c.48+1_48+2delinsGT	XP_016879161.1:n.48+1_48+2delinsGT
XM_017023673.2:c.48+1_48+2delinsGT	XP_016879162.1:n.48+1_48+2delinsGT
NM_024675.4:c.48+1_48+2delinsGT MANE Select	NP_078951.2:n.48+1_48+2delinsGT