Canonical Allele Identifier: CA7963672

Gene: PALB2

Linked Data

• dbSNP Id: rs759161292
• ExAC: 16:23641810 CACA / C
• gnomAD v2: 16-23641810-CACA-C
• gnomAD v3: 16-23630489-CACA-C
• gnomAD v4: 16-23630489-CACA-C
• MyVariant Identifiers: chr16:g.23641811_23641813del (hg19) ; chr16:g.23630490_23630492del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630491_23630493del , CM000678.2:g.23630491_23630493del	GRCh38
NC_000016.9:g.23641812_23641814del , CM000678.1:g.23641812_23641814del	GRCh37
NC_000016.8:g.23549313_23549315del	NCBI36
NG_007406.1:g.15866_15868del , LRG_308:g.15866_15868del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-23_1691-21del	ENSP00000460666.3:n.1691-23_1691-21del
ENST00000565038.2:c.212-1217_212-1215del	ENSP00000459882.2:n.212-1217_212-1215del
ENST00000566069.6:c.1685-23_1685-21del	ENSP00000459237.2:n.1685-23_1685-21del
ENST00000697377.2:c.1691-23_1691-21del	ENSP00000513286.2:n.1691-23_1691-21del
ENST00000697379.2:c.1691-23_1691-21del	ENSP00000513287.2:n.1691-23_1691-21del
ENST00000561514.2:c.800-23_800-21del	ENSP00000460666.2:n.800-23_800-21del
ENST00000697374.1:c.800-23_800-21del	ENSP00000513284.1:n.800-23_800-21del
ENST00000697375.1:n.3032-23_3032-21del
ENST00000697376.1:c.800-23_800-21del	ENSP00000513285.1:n.800-23_800-21del
ENST00000697377.1:c.800-23_800-21del	ENSP00000513286.1:n.800-23_800-21del
ENST00000697378.1:n.2205-23_2205-21del
ENST00000697379.1:c.800-23_800-21del	ENSP00000513287.1:n.800-23_800-21del
ENST00000697380.1:n.590_592del
ENST00000697381.1:n.380-23_380-21del
ENST00000697382.1:c.800-23_800-21del	ENSP00000513288.1:n.800-23_800-21del
ENST00000697383.1:c.49-1217_49-1215del	ENSP00000513289.1:n.49-1217_49-1215del
ENST00000697384.1:n.1839-23_1839-21del
ENST00000261584.9:c.1685-23_1685-21del MANE Select	ENSP00000261584.4:n.1685-23_1685-21del
ENST00000261584.8:c.1685-23_1685-21del	ENSP00000261584.4:n.1685-23_1685-21del
ENST00000565038.1:c.87-1217_87-1215del
ENST00000568219.5:c.800-23_800-21del	ENSP00000454703.2:n.800-23_800-21del
NM_024675.3:c.1685-23_1685-21del , LRG_308t1:c.1685-23_1685-21del	NP_078951.2:n.1685-23_1685-21del
XM_011545946.1:c.1691-23_1691-21del	XP_011544248.1:n.1691-23_1691-21del
XM_011545947.1:c.1691-23_1691-21del	XP_011544249.1:n.1691-23_1691-21del
XM_011545948.1:c.800-23_800-21del	XP_011544250.1:n.800-23_800-21del
XR_950851.1:n.2481-23_2481-21del
XM_011545946.2:c.1691-23_1691-21del	XP_011544248.1:n.1691-23_1691-21del
XM_011545947.2:c.1691-23_1691-21del	XP_011544249.1:n.1691-23_1691-21del
XM_011545948.2:c.800-23_800-21del	XP_011544250.1:n.800-23_800-21del
XM_017023671.1:c.1691-23_1691-21del	XP_016879160.1:n.1691-23_1691-21del
XM_017023672.2:c.1685-23_1685-21del	XP_016879161.1:n.1685-23_1685-21del
XM_017023673.2:c.1685-23_1685-21del	XP_016879162.1:n.1685-23_1685-21del
NM_024675.4:c.1685-23_1685-21del MANE Select	NP_078951.2:n.1685-23_1685-21del