Canonical Allele Identifier: CA719227201

Gene: PALB2

Linked Data

• dbSNP Id: rs1474211050
• gnomAD v3: 16-23621200-ACT-A
• gnomAD v4: 16-23621200-ACT-A
• MyVariant Identifiers: chr16:g.23632522_23632523del (hg19) ; chr16:g.23621201_23621202del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621203_23621204del , CM000678.2:g.23621203_23621204del	GRCh38
NC_000016.9:g.23632524_23632525del , CM000678.1:g.23632524_23632525del	GRCh37
NC_000016.8:g.23540025_23540026del	NCBI36
NG_007406.1:g.25156_25157del , LRG_308:g.25156_25157del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3119+160_3119+161del	ENSP00000460666.3:n.3119+160_3119+161del
ENST00000565038.2:c.*594+160_*594+161del	ENSP00000459882.2:n.*594+160_*594+161del
ENST00000566069.6:c.3113+160_3113+161del	ENSP00000459237.2:n.3113+160_3113+161del
ENST00000697377.2:c.2957+160_2957+161del	ENSP00000513286.2:n.2957+160_2957+161del
ENST00000697379.2:c.3119+160_3119+161del	ENSP00000513287.2:n.3119+160_3119+161del
ENST00000561514.2:c.2228+160_2228+161del	ENSP00000460666.2:n.2228+160_2228+161del
ENST00000697374.1:c.2228+160_2228+161del	ENSP00000513284.1:n.2228+160_2228+161del
ENST00000697375.1:n.4460+160_4460+161del
ENST00000697376.1:c.2228+160_2228+161del	ENSP00000513285.1:n.2228+160_2228+161del
ENST00000697377.1:c.2066+160_2066+161del	ENSP00000513286.1:n.2066+160_2066+161del
ENST00000697378.1:n.3633+160_3633+161del
ENST00000697379.1:c.2228+160_2228+161del	ENSP00000513287.1:n.2228+160_2228+161del
ENST00000697380.1:n.2405+160_2405+161del
ENST00000697381.1:n.1808+160_1808+161del
ENST00000697382.1:c.2228+160_2228+161del	ENSP00000513288.1:n.2228+160_2228+161del
ENST00000697383.1:c.647+160_647+161del	ENSP00000513289.1:n.647+160_647+161del
ENST00000261584.9:c.3113+160_3113+161del MANE Select	ENSP00000261584.4:n.3113+160_3113+161del
ENST00000261584.8:c.3113+160_3113+161del	ENSP00000261584.4:n.3113+160_3113+161del
ENST00000566069.5:c.28+160_28+161del
ENST00000568219.5:c.2228+160_2228+161del	ENSP00000454703.2:n.2228+160_2228+161del
NM_024675.3:c.3113+160_3113+161del , LRG_308t1:c.3113+160_3113+161del	NP_078951.2:n.3113+160_3113+161del
XM_011545946.1:c.3119+160_3119+161del	XP_011544248.1:n.3119+160_3119+161del
XM_011545947.1:c.3119+160_3119+161del	XP_011544249.1:n.3119+160_3119+161del
XM_011545948.1:c.2228+160_2228+161del	XP_011544250.1:n.2228+160_2228+161del
XR_950851.1:n.3909+160_3909+161del
XM_011545946.2:c.3119+160_3119+161del	XP_011544248.1:n.3119+160_3119+161del
XM_011545947.2:c.3119+160_3119+161del	XP_011544249.1:n.3119+160_3119+161del
XM_011545948.2:c.2228+160_2228+161del	XP_011544250.1:n.2228+160_2228+161del
XM_017023671.1:c.3119+160_3119+161del	XP_016879160.1:n.3119+160_3119+161del
XM_017023672.2:c.3113+160_3113+161del	XP_016879161.1:n.3113+160_3113+161del
XM_017023673.2:c.3113+160_3113+161del	XP_016879162.1:n.3113+160_3113+161del
NM_024675.4:c.3113+160_3113+161del MANE Select	NP_078951.2:n.3113+160_3113+161del