Canonical Allele Identifier: CA2213428044

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635066_23635067delinsTG , CM000678.2:g.23635066_23635067delinsTG	GRCh38
NC_000016.9:g.23646387_23646388delinsTG , CM000678.1:g.23646387_23646388delinsTG	GRCh37
NC_000016.8:g.23553888_23553889delinsTG	NCBI36
NG_007406.1:g.11291_11292delinsCA , LRG_308:g.11291_11292delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1485_1486delinsCA	ENSP00000460666.3:p.Pro495=
ENST00000565038.2:c.211+2783_211+2784delinsCA	ENSP00000459882.2:n.211+2783_211+2784delinsCA
ENST00000566069.6:c.1479_1480delinsCA	ENSP00000459237.2:p.Pro493=
ENST00000697377.2:c.1485_1486delinsCA	ENSP00000513286.2:p.Pro495=
ENST00000697379.2:c.1485_1486delinsCA	ENSP00000513287.2:p.Pro495=
ENST00000561514.2:c.594_595delinsCA	ENSP00000460666.2:p.Pro198=
ENST00000697374.1:c.594_595delinsCA	ENSP00000513284.1:p.Pro198=
ENST00000697375.1:n.2826_2827delinsCA
ENST00000697376.1:c.594_595delinsCA	ENSP00000513285.1:p.Pro198=
ENST00000697377.1:c.594_595delinsCA	ENSP00000513286.1:p.Pro198=
ENST00000697378.1:n.1999_2000delinsCA
ENST00000697379.1:c.594_595delinsCA	ENSP00000513287.1:p.Pro198=
ENST00000697382.1:c.594_595delinsCA	ENSP00000513288.1:p.Pro198=
ENST00000697383.1:c.49-5792_49-5791delinsCA	ENSP00000513289.1:n.49-5792_49-5791delinsCA
ENST00000697384.1:n.1633_1634delinsCA
ENST00000261584.9:c.1479_1480delinsCA MANE Select	ENSP00000261584.4:p.Pro493=
ENST00000261584.8:c.1479_1480delinsCA	ENSP00000261584.4:p.Pro493=
ENST00000565038.1:c.86+2783_86+2784delinsCA
ENST00000568219.5:c.594_595delinsCA	ENSP00000454703.2:p.Pro198=
NM_024675.3:c.1479_1480delinsCA , LRG_308t1:c.1479_1480delinsCA	NP_078951.2:p.Pro493=
XM_011545946.1:c.1485_1486delinsCA	XP_011544248.1:p.Pro495=
XM_011545947.1:c.1485_1486delinsCA	XP_011544249.1:p.Pro495=
XM_011545948.1:c.594_595delinsCA	XP_011544250.1:p.Pro198=
XR_950851.1:n.2275_2276delinsCA
XM_011545946.2:c.1485_1486delinsCA	XP_011544248.1:p.Pro495=
XM_011545947.2:c.1485_1486delinsCA	XP_011544249.1:p.Pro495=
XM_011545948.2:c.594_595delinsCA	XP_011544250.1:p.Pro198=
XM_017023671.1:c.1485_1486delinsCA	XP_016879160.1:p.Pro495=
XM_017023672.2:c.1479_1480delinsCA	XP_016879161.1:p.Pro493=
XM_017023673.2:c.1479_1480delinsCA	XP_016879162.1:p.Pro493=
NM_024675.4:c.1479_1480delinsCA MANE Select	NP_078951.2:p.Pro493=