Canonical Allele Identifier: CA2695222897

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607898dup , CM000678.2:g.23607898dup	GRCh38
NC_000016.9:g.23619219dup , CM000678.1:g.23619219dup	GRCh37
NC_000016.8:g.23526720dup	NCBI36
NG_007406.1:g.38460dup , LRG_308:g.38460dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3322dup	ENSP00000460666.3:p.Met1108AsnfsTer17
ENST00000565038.2:c.*797dup	ENSP00000459882.2:n.*797dup
ENST00000566069.6:c.3202-4229dup	ENSP00000459237.2:n.3202-4229dup
ENST00000697377.2:c.3160dup	ENSP00000513286.2:p.Met1054AsnfsTer17
ENST00000697379.2:c.3322dup	ENSP00000513287.2:p.Met1108AsnfsTer17
ENST00000561514.2:c.2431dup	ENSP00000460666.2:p.Met811AsnfsTer17
ENST00000697374.1:c.2431dup	ENSP00000513284.1:p.Met811AsnfsTer17
ENST00000697375.1:n.4663dup
ENST00000697376.1:c.2317-4229dup	ENSP00000513285.1:n.2317-4229dup
ENST00000697377.1:c.2269dup	ENSP00000513286.1:p.Met757AsnfsTer17
ENST00000697378.1:n.3836dup
ENST00000697379.1:c.2431dup	ENSP00000513287.1:p.Met811AsnfsTer17
ENST00000697380.1:n.2520dup
ENST00000697381.1:n.2011dup
ENST00000697382.1:c.*93dup	ENSP00000513288.1:n.*93dup
ENST00000697383.1:c.850dup	ENSP00000513289.1:p.Met284AsnfsTer17
ENST00000261584.9:c.3316dup MANE Select	ENSP00000261584.4:p.Met1106AsnfsTer17
ENST00000261584.8:c.3316dup	ENSP00000261584.4:p.Met1106AsnfsTer17
ENST00000566069.5:c.117-4229dup
ENST00000568219.5:c.2431dup	ENSP00000454703.2:p.Met811AsnfsTer17
NM_024675.3:c.3316dup , LRG_308t1:c.3316dup	NP_078951.2:p.Met1106AsnfsTer17
XM_011545946.1:c.3322dup	XP_011544248.1:p.Met1108AsnfsTer17
XM_011545947.1:c.3208-4229dup	XP_011544249.1:n.3208-4229dup
XM_011545948.1:c.2431dup	XP_011544250.1:p.Met811AsnfsTer17
XR_950851.1:n.4024dup
XM_011545946.2:c.3322dup	XP_011544248.1:p.Met1108AsnfsTer17
XM_011545947.2:c.3208-4229dup	XP_011544249.1:n.3208-4229dup
XM_011545948.2:c.2431dup	XP_011544250.1:p.Met811AsnfsTer17
XM_017023671.1:c.3120-4229dup	XP_016879160.1:n.3120-4229dup
XM_017023672.2:c.3114-4229dup	XP_016879161.1:n.3114-4229dup
XM_017023673.2:c.3202-4229dup	XP_016879162.1:n.3202-4229dup
NM_024675.4:c.3316dup MANE Select	NP_078951.2:p.Met1106AsnfsTer17