Canonical Allele Identifier: CA2695197606

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2673839
• ClinVar RCV Id: RCV003450456

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614085_23614148del , CM000678.2:g.23614085_23614148del	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3120-57_3126del
ENST00000565038.2:c.*595-57_*601del
ENST00000566069.6:c.3114-57_3120del
ENST00000697377.2:c.2958-57_2964del
ENST00000697379.2:c.3120-57_3126del
ENST00000561514.2:c.2229-57_2235del
ENST00000697374.1:c.2229-57_2235del
ENST00000697375.1:n.4461-57_4467del
ENST00000697376.1:c.2229-57_2235del
ENST00000697377.1:c.2067-57_2073del
ENST00000697378.1:n.3634-57_3640del
ENST00000697379.1:c.2229-57_2235del
ENST00000697380.1:n.2406-6136_2406-6073del
ENST00000697381.1:n.1809-57_1815del
ENST00000697382.1:c.2229-6136_2229-6073del	ENSP00000513288.1:n.2229-6136_2229-6073del
ENST00000697383.1:c.648-57_654del
ENST00000261584.9:c.3114-57_3120del
ENST00000261584.8:c.3114-57_3120del
ENST00000566069.5:c.29-57_35del
ENST00000568219.5:c.2229-57_2235del
NM_024675.3:c.3114-57_3120del , LRG_308t1:c.3114-57_3120del
XM_011545946.1:c.3120-57_3126del
XM_011545947.1:c.3120-57_3126del
XM_011545948.1:c.2229-57_2235del
XR_950851.1:n.3910-6136_3910-6073del
XM_011545946.2:c.3120-57_3126del
XM_011545947.2:c.3120-57_3126del
XM_011545948.2:c.2229-57_2235del
XM_017023671.1:c.3119+7214_3119+7277del	XP_016879160.1:n.3119+7214_3119+7277del
XM_017023672.2:c.3113+7214_3113+7277del	XP_016879161.1:n.3113+7214_3113+7277del
XM_017023673.2:c.3114-57_3120del
NM_024675.4:c.3114-57_3120del