Canonical Allele Identifier: CA3265662809

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637925_23638041del , CM000678.2:g.23637925_23638041del	GRCh38
NC_000016.9:g.23649246_23649362del , CM000678.1:g.23649246_23649362del	GRCh37
NC_000016.8:g.23556747_23556863del	NCBI36
NG_007406.1:g.8317_8433del , LRG_308:g.8317_8433del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.108+29_136del , LRG_308t1:c.108+29_136del
NM_024675.4:c.108+29_136del
ENST00000261584.8:c.108+29_136del
ENST00000261584.9:c.108+29_136del
ENST00000561514.1:c.114+29_142del
ENST00000561514.2:c.-778+29_-750del
ENST00000561514.3:c.114+29_142del
ENST00000565038.2:c.108+29_136del
ENST00000566069.6:c.108+29_136del
ENST00000567003.1:n.386+29_414del
ENST00000568219.5:c.-778+29_-750del
ENST00000697374.1:c.-778+29_-750del
ENST00000697375.1:n.1455+29_1483del
ENST00000697376.1:c.-814+29_-750del
ENST00000697377.1:c.-778+29_-750del
ENST00000697377.2:c.114+29_142del
ENST00000697378.1:n.628+29_656del
ENST00000697379.1:c.-778+29_-750del
ENST00000697379.2:c.114+29_142del
ENST00000697382.1:c.-778+29_-750del
ENST00000697383.1:c.48+3069_48+3185del	ENSP00000513289.1:n.48+3069_48+3185del
ENST00000697384.1:n.262+29_290del
XM_011545946.1:c.114+29_142del
XM_011545946.2:c.114+29_142del
XM_011545947.1:c.114+29_142del
XM_011545947.2:c.114+29_142del
XM_011545948.1:c.-778+29_-750del
XM_011545948.2:c.-778+29_-750del
XM_017023671.1:c.114+29_142del
XM_017023672.2:c.108+29_136del
XM_017023673.2:c.108+29_136del
XR_950851.1:n.904+29_932del