Canonical Allele Identifier: CA2213429637

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635532_23635546delinsTGGTAAGTTATTGTA , CM000678.2:g.23635532_23635546delinsTGGTAAGTTATTGTA	GRCh38
NC_000016.9:g.23646853_23646867delinsTGGTAAGTTATTGTA , CM000678.1:g.23646853_23646867delinsTGGTAAGTTATTGTA	GRCh37
NC_000016.8:g.23554354_23554368delinsTGGTAAGTTATTGTA	NCBI36
NG_007406.1:g.10812_10826delinsTACAATAACTTACCA , LRG_308:g.10812_10826delinsTACAATAACTTACCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1006_1020delinsTACAATAACTTACCA	ENSP00000460666.3:p.Tyr336=
ENST00000565038.2:c.211+2304_211+2318delinsTACAATAACTTACCA	ENSP00000459882.2:n.211+2304_211+2318delinsTACAATAACTTACCA
ENST00000566069.6:c.1000_1014delinsTACAATAACTTACCA	ENSP00000459237.2:p.Tyr334=
ENST00000697377.2:c.1006_1020delinsTACAATAACTTACCA	ENSP00000513286.2:p.Tyr336=
ENST00000697379.2:c.1006_1020delinsTACAATAACTTACCA	ENSP00000513287.2:p.Tyr336=
ENST00000561514.2:c.115_129delinsTACAATAACTTACCA	ENSP00000460666.2:p.Tyr39=
ENST00000697374.1:c.115_129delinsTACAATAACTTACCA	ENSP00000513284.1:p.Tyr39=
ENST00000697375.1:n.2347_2361delinsTACAATAACTTACCA
ENST00000697376.1:c.115_129delinsTACAATAACTTACCA	ENSP00000513285.1:p.Tyr39=
ENST00000697377.1:c.115_129delinsTACAATAACTTACCA	ENSP00000513286.1:p.Tyr39=
ENST00000697378.1:n.1520_1534delinsTACAATAACTTACCA
ENST00000697379.1:c.115_129delinsTACAATAACTTACCA	ENSP00000513287.1:p.Tyr39=
ENST00000697382.1:c.115_129delinsTACAATAACTTACCA	ENSP00000513288.1:p.Tyr39=
ENST00000697383.1:c.48+5564_48+5578delinsTACAATAACTTACCA	ENSP00000513289.1:n.48+5564_48+5578delinsTACAATAACTTACCA
ENST00000697384.1:n.1154_1168delinsTACAATAACTTACCA
ENST00000261584.9:c.1000_1014delinsTACAATAACTTACCA MANE Select	ENSP00000261584.4:p.Tyr334=
ENST00000261584.8:c.1000_1014delinsTACAATAACTTACCA	ENSP00000261584.4:p.Tyr334=
ENST00000565038.1:c.86+2304_86+2318delinsTACAATAACTTACCA
ENST00000568219.5:c.115_129delinsTACAATAACTTACCA	ENSP00000454703.2:p.Tyr39=
NM_024675.3:c.1000_1014delinsTACAATAACTTACCA , LRG_308t1:c.1000_1014delinsTACAATAACTTACCA	NP_078951.2:p.Tyr334=
XM_011545946.1:c.1006_1020delinsTACAATAACTTACCA	XP_011544248.1:p.Tyr336=
XM_011545947.1:c.1006_1020delinsTACAATAACTTACCA	XP_011544249.1:p.Tyr336=
XM_011545948.1:c.115_129delinsTACAATAACTTACCA	XP_011544250.1:p.Tyr39=
XR_950851.1:n.1796_1810delinsTACAATAACTTACCA
XM_011545946.2:c.1006_1020delinsTACAATAACTTACCA	XP_011544248.1:p.Tyr336=
XM_011545947.2:c.1006_1020delinsTACAATAACTTACCA	XP_011544249.1:p.Tyr336=
XM_011545948.2:c.115_129delinsTACAATAACTTACCA	XP_011544250.1:p.Tyr39=
XM_017023671.1:c.1006_1020delinsTACAATAACTTACCA	XP_016879160.1:p.Tyr336=
XM_017023672.2:c.1000_1014delinsTACAATAACTTACCA	XP_016879161.1:p.Tyr334=
XM_017023673.2:c.1000_1014delinsTACAATAACTTACCA	XP_016879162.1:p.Tyr334=
NM_024675.4:c.1000_1014delinsTACAATAACTTACCA MANE Select	NP_078951.2:p.Tyr334=