Canonical Allele Identifier: CA621335402

Gene: PALB2

Linked Data

• dbSNP Id: rs1369095966
• gnomAD v2: 16-23647681-CTT-C
• gnomAD v3: 16-23636360-CTT-C
• gnomAD v4: 16-23636360-CTT-C
• MyVariant Identifiers: chr16:g.23647682_23647683del (hg19) ; chr16:g.23636361_23636362del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636361_23636362del , CM000678.2:g.23636361_23636362del	GRCh38
NC_000016.9:g.23647682_23647683del , CM000678.1:g.23647682_23647683del	GRCh37
NC_000016.8:g.23555183_23555184del	NCBI36
NG_007406.1:g.9996_9997del , LRG_308:g.9996_9997del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.218-28_218-27del	ENSP00000460666.3:n.218-28_218-27del
ENST00000565038.2:c.211+1488_211+1489del	ENSP00000459882.2:n.211+1488_211+1489del
ENST00000566069.6:c.212-28_212-27del	ENSP00000459237.2:n.212-28_212-27del
ENST00000697377.2:c.218-28_218-27del	ENSP00000513286.2:n.218-28_218-27del
ENST00000697379.2:c.218-28_218-27del	ENSP00000513287.2:n.218-28_218-27del
ENST00000561514.2:c.-674-28_-674-27del	ENSP00000460666.2:n.-674-28_-674-27del
ENST00000697374.1:c.-674-28_-674-27del	ENSP00000513284.1:n.-674-28_-674-27del
ENST00000697375.1:n.1559-28_1559-27del
ENST00000697376.1:c.-674-28_-674-27del	ENSP00000513285.1:n.-674-28_-674-27del
ENST00000697377.1:c.-674-28_-674-27del	ENSP00000513286.1:n.-674-28_-674-27del
ENST00000697378.1:n.732-28_732-27del
ENST00000697379.1:c.-674-28_-674-27del	ENSP00000513287.1:n.-674-28_-674-27del
ENST00000697382.1:c.-674-28_-674-27del	ENSP00000513288.1:n.-674-28_-674-27del
ENST00000697383.1:c.48+4748_48+4749del	ENSP00000513289.1:n.48+4748_48+4749del
ENST00000697384.1:n.366-28_366-27del
ENST00000261584.9:c.212-28_212-27del MANE Select	ENSP00000261584.4:n.212-28_212-27del
ENST00000261584.8:c.212-28_212-27del	ENSP00000261584.4:n.212-28_212-27del
ENST00000561514.1:c.218-28_218-27del	ENSP00000460666.1:n.218-28_218-27del
ENST00000565038.1:c.86+1488_86+1489del
ENST00000567003.1:n.490-28_490-27del
ENST00000568219.5:c.-674-28_-674-27del	ENSP00000454703.2:n.-674-28_-674-27del
NM_024675.3:c.212-28_212-27del , LRG_308t1:c.212-28_212-27del	NP_078951.2:n.212-28_212-27del
XM_011545946.1:c.218-28_218-27del	XP_011544248.1:n.218-28_218-27del
XM_011545947.1:c.218-28_218-27del	XP_011544249.1:n.218-28_218-27del
XM_011545948.1:c.-674-28_-674-27del	XP_011544250.1:n.-674-28_-674-27del
XR_950851.1:n.1008-28_1008-27del
XM_011545946.2:c.218-28_218-27del	XP_011544248.1:n.218-28_218-27del
XM_011545947.2:c.218-28_218-27del	XP_011544249.1:n.218-28_218-27del
XM_011545948.2:c.-674-28_-674-27del	XP_011544250.1:n.-674-28_-674-27del
XM_017023671.1:c.218-28_218-27del	XP_016879160.1:n.218-28_218-27del
XM_017023672.2:c.212-28_212-27del	XP_016879161.1:n.212-28_212-27del
XM_017023673.2:c.212-28_212-27del	XP_016879162.1:n.212-28_212-27del
NM_024675.4:c.212-28_212-27del MANE Select	NP_078951.2:n.212-28_212-27del