Canonical Allele Identifier: CA2582342507

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2587416
• ClinVar RCV Id: RCV003360866

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614039_23614645del , CM000678.2:g.23614039_23614645del	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3120-554_3172del
ENST00000565038.2:c.*595-554_*647del
ENST00000566069.6:c.3114-554_3166del
ENST00000697377.2:c.2958-554_3010del
ENST00000697379.2:c.3120-554_3172del
ENST00000561514.2:c.2229-554_2281del
ENST00000697374.1:c.2229-554_2281del
ENST00000697375.1:n.4461-554_4513del
ENST00000697376.1:c.2229-554_2281del
ENST00000697377.1:c.2067-554_2119del
ENST00000697378.1:n.3634-554_3686del
ENST00000697379.1:c.2229-554_2281del
ENST00000697380.1:n.2406-6633_2406-6027del
ENST00000697381.1:n.1809-554_1861del
ENST00000697382.1:c.2229-6633_2229-6027del	ENSP00000513288.1:n.2229-6633_2229-6027del
ENST00000697383.1:c.648-554_700del
ENST00000261584.9:c.3114-554_3166del
ENST00000261584.8:c.3114-554_3166del
ENST00000566069.5:c.29-554_81del
ENST00000568219.5:c.2229-554_2281del
NM_024675.3:c.3114-554_3166del , LRG_308t1:c.3114-554_3166del
XM_011545946.1:c.3120-554_3172del
XM_011545947.1:c.3120-554_3172del
XM_011545948.1:c.2229-554_2281del
XR_950851.1:n.3910-6633_3910-6027del
XM_011545946.2:c.3120-554_3172del
XM_011545947.2:c.3120-554_3172del
XM_011545948.2:c.2229-554_2281del
XM_017023671.1:c.3119+6717_3119+7323del	XP_016879160.1:n.3119+6717_3119+7323del
XM_017023672.2:c.3113+6717_3113+7323del	XP_016879161.1:n.3113+6717_3113+7323del
XM_017023673.2:c.3114-554_3166del
NM_024675.4:c.3114-554_3166del