Canonical Allele Identifier: CA3265662808

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637919_23638106del , CM000678.2:g.23637919_23638106del	GRCh38
NC_000016.9:g.23649240_23649427del , CM000678.1:g.23649240_23649427del	GRCh37
NC_000016.8:g.23556741_23556928del	NCBI36
NG_007406.1:g.8252_8439del , LRG_308:g.8252_8439del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.72_142del , LRG_308t1:c.72_142del
NM_024675.4:c.72_142del
ENST00000261584.8:c.72_142del
ENST00000261584.9:c.72_142del
ENST00000561514.1:c.78_148del
ENST00000561514.2:c.-814_-744del
ENST00000561514.3:c.78_148del
ENST00000565038.2:c.72_142del
ENST00000566069.6:c.72_142del
ENST00000567003.1:n.350_420del
ENST00000568219.5:c.-814_-744del
ENST00000697374.1:c.-814_-744del
ENST00000697375.1:n.1419_1489del
ENST00000697376.1:c.-850_-744del
ENST00000697377.1:c.-814_-744del
ENST00000697377.2:c.78_148del
ENST00000697378.1:n.592_662del
ENST00000697379.1:c.-814_-744del
ENST00000697379.2:c.78_148del
ENST00000697382.1:c.-814_-744del
ENST00000697383.1:c.48+3004_48+3191del	ENSP00000513289.1:n.48+3004_48+3191del
ENST00000697384.1:n.226_296del
XM_011545946.1:c.78_148del
XM_011545946.2:c.78_148del
XM_011545947.1:c.78_148del
XM_011545947.2:c.78_148del
XM_011545948.1:c.-814_-744del
XM_011545948.2:c.-814_-744del
XM_017023671.1:c.78_148del
XM_017023672.2:c.72_142del
XM_017023673.2:c.72_142del
XR_950851.1:n.868_938del