Canonical Allele Identifier: CA2632331009

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641172-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641172A>T , CM000678.2:g.23641172A>T	GRCh38
NC_000016.9:g.23652493A>T , CM000678.1:g.23652493A>T	GRCh37
NC_000016.8:g.23559994A>T	NCBI36
NG_007406.1:g.5186T>A , LRG_308:g.5186T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-867T>A	ENSP00000460666.3:n.-867T>A
ENST00000565038.2:c.-15T>A	ENSP00000459882.2:n.-15T>A
ENST00000566069.6:c.-15T>A	ENSP00000459237.2:n.-15T>A
ENST00000697377.2:c.-254T>A	ENSP00000513286.2:n.-254T>A
ENST00000697379.2:c.-160T>A	ENSP00000513287.2:n.-160T>A
ENST00000561514.2:c.-1758T>A	ENSP00000460666.2:n.-1758T>A
ENST00000697374.1:c.-1349T>A	ENSP00000513284.1:n.-1349T>A
ENST00000697376.1:c.-1070T>A	ENSP00000513285.1:n.-1070T>A
ENST00000697377.1:c.-1145T>A	ENSP00000513286.1:n.-1145T>A
ENST00000697379.1:c.-1051T>A	ENSP00000513287.1:n.-1051T>A
ENST00000697382.1:c.-1809T>A	ENSP00000513288.1:n.-1809T>A
ENST00000697383.1:c.-15T>A	ENSP00000513289.1:n.-15T>A
ENST00000697384.1:n.140T>A
ENST00000261584.9:c.-15T>A MANE Select	ENSP00000261584.4:n.-15T>A
ENST00000261584.8:c.-15T>A	ENSP00000261584.4:n.-15T>A
ENST00000567003.1:n.130T>A
ENST00000568219.5:c.-883T>A	ENSP00000454703.2:n.-883T>A
NM_024675.3:c.-15T>A , LRG_308t1:c.-15T>A	NP_078951.2:n.-15T>A
XM_011545948.1:c.-1034T>A	XP_011544250.1:n.-1034T>A
XM_011545946.2:c.-867T>A	XP_011544248.1:n.-867T>A
XM_011545947.2:c.-867T>A	XP_011544249.1:n.-867T>A
XM_011545948.2:c.-1034T>A	XP_011544250.1:n.-1034T>A
XM_017023671.1:c.-867T>A	XP_016879160.1:n.-867T>A
XM_017023672.2:c.-15T>A	XP_016879161.1:n.-15T>A
XM_017023673.2:c.-15T>A	XP_016879162.1:n.-15T>A
NM_024675.4:c.-15T>A MANE Select	NP_078951.2:n.-15T>A