Canonical Allele Identifier: CA7963675

Gene: PALB2

Linked Data

• dbSNP Id: rs767535890
• ExAC: 16:23641820 TAACAAAACCC / T
• gnomAD v2: 16-23641820-TAACAAAACCC-T
• gnomAD v4: 16-23630499-TAACAAAACCC-T
• MyVariant Identifiers: chr16:g.23641821_23641830del (hg19) ; chr16:g.23630500_23630509del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630508_23630517del , CM000678.2:g.23630508_23630517del	GRCh38
NC_000016.9:g.23641829_23641838del , CM000678.1:g.23641829_23641838del	GRCh37
NC_000016.8:g.23549330_23549339del	NCBI36
NG_007406.1:g.15849_15858del , LRG_308:g.15849_15858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-40_1691-31del	ENSP00000460666.3:n.1691-40_1691-31del
ENST00000565038.2:c.212-1234_212-1225del	ENSP00000459882.2:n.212-1234_212-1225del
ENST00000566069.6:c.1685-40_1685-31del	ENSP00000459237.2:n.1685-40_1685-31del
ENST00000697377.2:c.1691-40_1691-31del	ENSP00000513286.2:n.1691-40_1691-31del
ENST00000697379.2:c.1691-40_1691-31del	ENSP00000513287.2:n.1691-40_1691-31del
ENST00000561514.2:c.800-40_800-31del	ENSP00000460666.2:n.800-40_800-31del
ENST00000697374.1:c.800-40_800-31del	ENSP00000513284.1:n.800-40_800-31del
ENST00000697375.1:n.3032-40_3032-31del
ENST00000697376.1:c.800-40_800-31del	ENSP00000513285.1:n.800-40_800-31del
ENST00000697377.1:c.800-40_800-31del	ENSP00000513286.1:n.800-40_800-31del
ENST00000697378.1:n.2205-40_2205-31del
ENST00000697379.1:c.800-40_800-31del	ENSP00000513287.1:n.800-40_800-31del
ENST00000697380.1:n.573_582del
ENST00000697381.1:n.380-40_380-31del
ENST00000697382.1:c.800-40_800-31del	ENSP00000513288.1:n.800-40_800-31del
ENST00000697383.1:c.49-1234_49-1225del	ENSP00000513289.1:n.49-1234_49-1225del
ENST00000697384.1:n.1839-40_1839-31del
ENST00000261584.9:c.1685-40_1685-31del MANE Select	ENSP00000261584.4:n.1685-40_1685-31del
ENST00000261584.8:c.1685-40_1685-31del	ENSP00000261584.4:n.1685-40_1685-31del
ENST00000565038.1:c.87-1234_87-1225del
ENST00000568219.5:c.800-40_800-31del	ENSP00000454703.2:n.800-40_800-31del
NM_024675.3:c.1685-40_1685-31del , LRG_308t1:c.1685-40_1685-31del	NP_078951.2:n.1685-40_1685-31del
XM_011545946.1:c.1691-40_1691-31del	XP_011544248.1:n.1691-40_1691-31del
XM_011545947.1:c.1691-40_1691-31del	XP_011544249.1:n.1691-40_1691-31del
XM_011545948.1:c.800-40_800-31del	XP_011544250.1:n.800-40_800-31del
XR_950851.1:n.2481-40_2481-31del
XM_011545946.2:c.1691-40_1691-31del	XP_011544248.1:n.1691-40_1691-31del
XM_011545947.2:c.1691-40_1691-31del	XP_011544249.1:n.1691-40_1691-31del
XM_011545948.2:c.800-40_800-31del	XP_011544250.1:n.800-40_800-31del
XM_017023671.1:c.1691-40_1691-31del	XP_016879160.1:n.1691-40_1691-31del
XM_017023672.2:c.1685-40_1685-31del	XP_016879161.1:n.1685-40_1685-31del
XM_017023673.2:c.1685-40_1685-31del	XP_016879162.1:n.1685-40_1685-31del
NM_024675.4:c.1685-40_1685-31del MANE Select	NP_078951.2:n.1685-40_1685-31del