Canonical Allele Identifier: CA621661741

Gene: PALB2

Linked Data

• dbSNP Id: rs1408830355
• gnomAD v2: 16-23646105-G-GA
• gnomAD v3: 16-23634784-G-GA
• gnomAD v4: 16-23634784-G-GA
• MyVariant Identifiers: chr16:g.23646105_23646106insA (hg19) ; chr16:g.23634784_23634785insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634788dup , CM000678.2:g.23634788dup	GRCh38
NC_000016.9:g.23646109dup , CM000678.1:g.23646109dup	GRCh37
NC_000016.8:g.23553610dup	NCBI36
NG_007406.1:g.11573dup , LRG_308:g.11573dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1690+77dup	ENSP00000460666.3:n.1690+77dup
ENST00000565038.2:c.211+3065dup	ENSP00000459882.2:n.211+3065dup
ENST00000566069.6:c.1684+77dup	ENSP00000459237.2:n.1684+77dup
ENST00000697377.2:c.1690+77dup	ENSP00000513286.2:n.1690+77dup
ENST00000697379.2:c.1690+77dup	ENSP00000513287.2:n.1690+77dup
ENST00000561514.2:c.799+77dup	ENSP00000460666.2:n.799+77dup
ENST00000697374.1:c.799+77dup	ENSP00000513284.1:n.799+77dup
ENST00000697375.1:n.3031+77dup
ENST00000697376.1:c.799+77dup	ENSP00000513285.1:n.799+77dup
ENST00000697377.1:c.799+77dup	ENSP00000513286.1:n.799+77dup
ENST00000697378.1:n.2204+77dup
ENST00000697379.1:c.799+77dup	ENSP00000513287.1:n.799+77dup
ENST00000697382.1:c.799+77dup	ENSP00000513288.1:n.799+77dup
ENST00000697383.1:c.49-5510dup	ENSP00000513289.1:n.49-5510dup
ENST00000697384.1:n.1838+77dup
ENST00000261584.9:c.1684+77dup MANE Select	ENSP00000261584.4:n.1684+77dup
ENST00000261584.8:c.1684+77dup	ENSP00000261584.4:n.1684+77dup
ENST00000565038.1:c.86+3065dup
ENST00000568219.5:c.799+77dup	ENSP00000454703.2:n.799+77dup
NM_024675.3:c.1684+77dup , LRG_308t1:c.1684+77dup	NP_078951.2:n.1684+77dup
XM_011545946.1:c.1690+77dup	XP_011544248.1:n.1690+77dup
XM_011545947.1:c.1690+77dup	XP_011544249.1:n.1690+77dup
XM_011545948.1:c.799+77dup	XP_011544250.1:n.799+77dup
XR_950851.1:n.2480+77dup
XM_011545946.2:c.1690+77dup	XP_011544248.1:n.1690+77dup
XM_011545947.2:c.1690+77dup	XP_011544249.1:n.1690+77dup
XM_011545948.2:c.799+77dup	XP_011544250.1:n.799+77dup
XM_017023671.1:c.1690+77dup	XP_016879160.1:n.1690+77dup
XM_017023672.2:c.1684+77dup	XP_016879161.1:n.1684+77dup
XM_017023673.2:c.1684+77dup	XP_016879162.1:n.1684+77dup
NM_024675.4:c.1684+77dup MANE Select	NP_078951.2:n.1684+77dup