Canonical Allele Identifier: CA2739266669

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2832739
• ClinVar RCV Id: RCV003608096

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641143_23641161del , CM000678.2:g.23641143_23641161del	GRCh38
NC_000016.9:g.23652464_23652482del , CM000678.1:g.23652464_23652482del	GRCh37
NC_000016.8:g.23559965_23559983del	NCBI36
NG_007406.1:g.5197_5215del , LRG_308:g.5197_5215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-856_-838del	ENSP00000460666.3:n.-856_-838del
ENST00000565038.2:c.-4_15del
ENST00000566069.6:c.-4_15del
ENST00000697377.2:c.-243_-225del	ENSP00000513286.2:n.-243_-225del
ENST00000697379.2:c.-149_-131del	ENSP00000513287.2:n.-149_-131del
ENST00000561514.2:c.-1747_-1729del	ENSP00000460666.2:n.-1747_-1729del
ENST00000697374.1:c.-1338_-1320del	ENSP00000513284.1:n.-1338_-1320del
ENST00000697376.1:c.-1059_-1041del	ENSP00000513285.1:n.-1059_-1041del
ENST00000697377.1:c.-1134_-1116del	ENSP00000513286.1:n.-1134_-1116del
ENST00000697379.1:c.-1040_-1022del	ENSP00000513287.1:n.-1040_-1022del
ENST00000697382.1:c.-1798_-1780del	ENSP00000513288.1:n.-1798_-1780del
ENST00000697383.1:c.-4_15del
ENST00000697384.1:n.151_169del
ENST00000261584.9:c.-4_15del
ENST00000261584.8:c.-4_15del
ENST00000567003.1:n.141_159del
ENST00000568219.5:c.-872_-854del	ENSP00000454703.2:n.-872_-854del
NM_024675.3:c.-4_15del , LRG_308t1:c.-4_15del
XM_011545948.1:c.-1023_-1005del	XP_011544250.1:n.-1023_-1005del
XM_011545946.2:c.-856_-838del	XP_011544248.1:n.-856_-838del
XM_011545947.2:c.-856_-838del	XP_011544249.1:n.-856_-838del
XM_011545948.2:c.-1023_-1005del	XP_011544250.1:n.-1023_-1005del
XM_017023671.1:c.-856_-838del	XP_016879160.1:n.-856_-838del
XM_017023672.2:c.-4_15del
XM_017023673.2:c.-4_15del
NM_024675.4:c.-4_15del