Canonical Allele Identifier: CA916081816

Gene: PALB2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623063_23623077del , CM000678.2:g.23623063_23623077del	GRCh38
NC_000016.9:g.23634384_23634398del , CM000678.1:g.23634384_23634398del	GRCh37
NC_000016.8:g.23541885_23541899del	NCBI36
NG_007406.1:g.23284_23298del , LRG_308:g.23284_23298del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2897_2911del	ENSP00000460666.3:p.Gly966_Ala970del
ENST00000565038.2:c.*372_*386del	ENSP00000459882.2:n.*372_*386del
ENST00000566069.6:c.2891_2905del	ENSP00000459237.2:p.Gly964_Ala968del
ENST00000697377.2:c.2735_2749del	ENSP00000513286.2:p.Gly912_Ala916del
ENST00000697379.2:c.2897_2911del	ENSP00000513287.2:p.Gly966_Ala970del
ENST00000561514.2:c.2006_2020del	ENSP00000460666.2:p.Gly669_Ala673del
ENST00000697374.1:c.2006_2020del	ENSP00000513284.1:p.Gly669_Ala673del
ENST00000697375.1:n.4238_4252del
ENST00000697376.1:c.2006_2020del	ENSP00000513285.1:p.Gly669_Ala673del
ENST00000697377.1:c.1844_1858del	ENSP00000513286.1:p.Gly615_Ala619del
ENST00000697378.1:n.3411_3425del
ENST00000697379.1:c.2006_2020del	ENSP00000513287.1:p.Gly669_Ala673del
ENST00000697380.1:n.2183_2197del
ENST00000697381.1:n.1586_1600del
ENST00000697382.1:c.2006_2020del	ENSP00000513288.1:p.Gly669_Ala673del
ENST00000697383.1:c.425_439del	ENSP00000513289.1:p.Gly142_Ala146del
ENST00000261584.9:c.2891_2905del MANE Select	ENSP00000261584.4:p.Gly964_Ala968del
ENST00000261584.8:c.2891_2905del	ENSP00000261584.4:p.Gly964_Ala968del
ENST00000568219.5:c.2006_2020del	ENSP00000454703.2:p.Gly669_Ala673del
NM_024675.3:c.2891_2905del , LRG_308t1:c.2891_2905del	NP_078951.2:p.Gly964_Ala968del
XM_011545946.1:c.2897_2911del	XP_011544248.1:p.Gly966_Ala970del
XM_011545947.1:c.2897_2911del	XP_011544249.1:p.Gly966_Ala970del
XM_011545948.1:c.2006_2020del	XP_011544250.1:p.Gly669_Ala673del
XR_950851.1:n.3687_3701del
XM_011545946.2:c.2897_2911del	XP_011544248.1:p.Gly966_Ala970del
XM_011545947.2:c.2897_2911del	XP_011544249.1:p.Gly966_Ala970del
XM_011545948.2:c.2006_2020del	XP_011544250.1:p.Gly669_Ala673del
XM_017023671.1:c.2897_2911del	XP_016879160.1:p.Gly966_Ala970del
XM_017023672.2:c.2891_2905del	XP_016879161.1:p.Gly964_Ala968del
XM_017023673.2:c.2891_2905del	XP_016879162.1:p.Gly964_Ala968del
NM_024675.4:c.2891_2905del MANE Select	NP_078951.2:p.Gly964_Ala968del