Canonical Allele Identifier: CA2213436394

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641086_23641088delinsCCG , CM000678.2:g.23641086_23641088delinsCCG	GRCh38
NC_000016.9:g.23652407_23652409delinsCCG , CM000678.1:g.23652407_23652409delinsCCG	GRCh37
NC_000016.8:g.23559908_23559910delinsCCG	NCBI36
NG_007406.1:g.5270_5272delinsCGG , LRG_308:g.5270_5272delinsCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-783_-781delinsCGG	ENSP00000460666.3:n.-783_-781delinsCGG
ENST00000565038.2:c.48+22_48+24delinsCGG	ENSP00000459882.2:n.48+22_48+24delinsCGG
ENST00000566069.6:c.48+22_48+24delinsCGG	ENSP00000459237.2:n.48+22_48+24delinsCGG
ENST00000697377.2:c.-192+22_-192+24delinsCGG	ENSP00000513286.2:n.-192+22_-192+24delinsCGG
ENST00000697379.2:c.-98+22_-98+24delinsCGG	ENSP00000513287.2:n.-98+22_-98+24delinsCGG
ENST00000561514.2:c.-1674_-1672delinsCGG	ENSP00000460666.2:n.-1674_-1672delinsCGG
ENST00000697374.1:c.-1265_-1263delinsCGG	ENSP00000513284.1:n.-1265_-1263delinsCGG
ENST00000697376.1:c.-1008+22_-1008+24delinsCGG	ENSP00000513285.1:n.-1008+22_-1008+24delinsCGG
ENST00000697377.1:c.-1083+22_-1083+24delinsCGG	ENSP00000513286.1:n.-1083+22_-1083+24delinsCGG
ENST00000697379.1:c.-989+22_-989+24delinsCGG	ENSP00000513287.1:n.-989+22_-989+24delinsCGG
ENST00000697382.1:c.-1725_-1723delinsCGG	ENSP00000513288.1:n.-1725_-1723delinsCGG
ENST00000697383.1:c.48+22_48+24delinsCGG	ENSP00000513289.1:n.48+22_48+24delinsCGG
ENST00000697384.1:n.202+22_202+24delinsCGG
ENST00000261584.9:c.48+22_48+24delinsCGG MANE Select	ENSP00000261584.4:n.48+22_48+24delinsCGG
ENST00000261584.8:c.48+22_48+24delinsCGG	ENSP00000261584.4:n.48+22_48+24delinsCGG
ENST00000567003.1:n.192+22_192+24delinsCGG
ENST00000568219.5:c.-838+39_-838+41delinsCGG	ENSP00000454703.2:n.-838+39_-838+41delinsCGG
NM_024675.3:c.48+22_48+24delinsCGG , LRG_308t1:c.48+22_48+24delinsCGG	NP_078951.2:n.48+22_48+24delinsCGG
XM_011545946.1:c.-783_-781delinsCGG	XP_011544248.1:n.-783_-781delinsCGG
XM_011545947.1:c.-783_-781delinsCGG	XP_011544249.1:n.-783_-781delinsCGG
XM_011545948.1:c.-972+22_-972+24delinsCGG	XP_011544250.1:n.-972+22_-972+24delinsCGG
XR_950851.1:n.8_10delinsCGG
XM_011545946.2:c.-783_-781delinsCGG	XP_011544248.1:n.-783_-781delinsCGG
XM_011545947.2:c.-783_-781delinsCGG	XP_011544249.1:n.-783_-781delinsCGG
XM_011545948.2:c.-972+22_-972+24delinsCGG	XP_011544250.1:n.-972+22_-972+24delinsCGG
XM_017023671.1:c.-783_-781delinsCGG	XP_016879160.1:n.-783_-781delinsCGG
XM_017023672.2:c.48+22_48+24delinsCGG	XP_016879161.1:n.48+22_48+24delinsCGG
XM_017023673.2:c.48+22_48+24delinsCGG	XP_016879162.1:n.48+22_48+24delinsCGG
NM_024675.4:c.48+22_48+24delinsCGG MANE Select	NP_078951.2:n.48+22_48+24delinsCGG