Canonical Allele Identifier: CA975710689

Gene: PALB2

Linked Data

• gnomAD v3: 16-23636333-TTCTGAGGAGG-T
• gnomAD v4: 16-23636333-TTCTGAGGAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636334_23636343del , CM000678.2:g.23636334_23636343del	GRCh38
NC_000016.9:g.23647655_23647664del , CM000678.1:g.23647655_23647664del	GRCh37
NC_000016.8:g.23555156_23555165del	NCBI36
NG_007406.1:g.10015_10024del , LRG_308:g.10015_10024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.218-9_218del
ENST00000565038.2:c.211+1507_211+1516del	ENSP00000459882.2:n.211+1507_211+1516del
ENST00000566069.6:c.212-9_212del
ENST00000697377.2:c.218-9_218del
ENST00000697379.2:c.218-9_218del
ENST00000561514.2:c.-674-9_-674del
ENST00000697374.1:c.-674-9_-674del
ENST00000697375.1:n.1559-9_1559del
ENST00000697376.1:c.-674-9_-674del
ENST00000697377.1:c.-674-9_-674del
ENST00000697378.1:n.732-9_732del
ENST00000697379.1:c.-674-9_-674del
ENST00000697382.1:c.-674-9_-674del
ENST00000697383.1:c.48+4767_48+4776del	ENSP00000513289.1:n.48+4767_48+4776del
ENST00000697384.1:n.366-9_366del
ENST00000261584.9:c.212-9_212del
ENST00000261584.8:c.212-9_212del
ENST00000561514.1:c.218-9_218del
ENST00000565038.1:c.86+1507_86+1516del
ENST00000567003.1:n.490-9_490del
ENST00000568219.5:c.-674-9_-674del
NM_024675.3:c.212-9_212del , LRG_308t1:c.212-9_212del
XM_011545946.1:c.218-9_218del
XM_011545947.1:c.218-9_218del
XM_011545948.1:c.-674-9_-674del
XR_950851.1:n.1008-9_1008del
XM_011545946.2:c.218-9_218del
XM_011545947.2:c.218-9_218del
XM_011545948.2:c.-674-9_-674del
XM_017023671.1:c.218-9_218del
XM_017023672.2:c.212-9_212del
XM_017023673.2:c.212-9_212del
NM_024675.4:c.212-9_212del