Canonical Allele Identifier: CA2632327681

Gene: PALB2

Linked Data

• gnomAD v4: 16-23630490-A-AGGCCGGGCGCGGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630490_23630491insGGCCGGGCGCGGTGG , CM000678.2:g.23630490_23630491insGGCCGGGCGCGGTGG	GRCh38
NC_000016.9:g.23641811_23641812insGGCCGGGCGCGGTGG , CM000678.1:g.23641811_23641812insGGCCGGGCGCGGTGG	GRCh37
NC_000016.8:g.23549312_23549313insGGCCGGGCGCGGTGG	NCBI36
NG_007406.1:g.15867_15868insCCACCGCGCCCGGCC , LRG_308:g.15867_15868insCCACCGCGCCCGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-22_1691-21insCCACCGCGCCCGGCC	ENSP00000460666.3:n.1691-22_1691-21insCCACCGCGCCCGGCC
ENST00000565038.2:c.212-1216_212-1215insCCACCGCGCCCGGCC	ENSP00000459882.2:n.212-1216_212-1215insCCACCGCGCCCGGCC
ENST00000566069.6:c.1685-22_1685-21insCCACCGCGCCCGGCC	ENSP00000459237.2:n.1685-22_1685-21insCCACCGCGCCCGGCC
ENST00000697377.2:c.1691-22_1691-21insCCACCGCGCCCGGCC	ENSP00000513286.2:n.1691-22_1691-21insCCACCGCGCCCGGCC
ENST00000697379.2:c.1691-22_1691-21insCCACCGCGCCCGGCC	ENSP00000513287.2:n.1691-22_1691-21insCCACCGCGCCCGGCC
ENST00000561514.2:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000460666.2:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697374.1:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000513284.1:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697375.1:n.3032-22_3032-21insCCACCGCGCCCGGCC
ENST00000697376.1:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000513285.1:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697377.1:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000513286.1:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697378.1:n.2205-22_2205-21insCCACCGCGCCCGGCC
ENST00000697379.1:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000513287.1:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697380.1:n.591_592insCCACCGCGCCCGGCC
ENST00000697381.1:n.380-22_380-21insCCACCGCGCCCGGCC
ENST00000697382.1:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000513288.1:n.800-22_800-21insCCACCGCGCCCGGCC
ENST00000697383.1:c.49-1216_49-1215insCCACCGCGCCCGGCC	ENSP00000513289.1:n.49-1216_49-1215insCCACCGCGCCCGGCC
ENST00000697384.1:n.1839-22_1839-21insCCACCGCGCCCGGCC
ENST00000261584.9:c.1685-22_1685-21insCCACCGCGCCCGGCC MANE Select	ENSP00000261584.4:n.1685-22_1685-21insCCACCGCGCCCGGCC
ENST00000261584.8:c.1685-22_1685-21insCCACCGCGCCCGGCC	ENSP00000261584.4:n.1685-22_1685-21insCCACCGCGCCCGGCC
ENST00000565038.1:c.87-1216_87-1215insCCACCGCGCCCGGCC
ENST00000568219.5:c.800-22_800-21insCCACCGCGCCCGGCC	ENSP00000454703.2:n.800-22_800-21insCCACCGCGCCCGGCC
NM_024675.3:c.1685-22_1685-21insCCACCGCGCCCGGCC , LRG_308t1:c.1685-22_1685-21insCCACCGCGCCCGGCC	NP_078951.2:n.1685-22_1685-21insCCACCGCGCCCGGCC
XM_011545946.1:c.1691-22_1691-21insCCACCGCGCCCGGCC	XP_011544248.1:n.1691-22_1691-21insCCACCGCGCCCGGCC
XM_011545947.1:c.1691-22_1691-21insCCACCGCGCCCGGCC	XP_011544249.1:n.1691-22_1691-21insCCACCGCGCCCGGCC
XM_011545948.1:c.800-22_800-21insCCACCGCGCCCGGCC	XP_011544250.1:n.800-22_800-21insCCACCGCGCCCGGCC
XR_950851.1:n.2481-22_2481-21insCCACCGCGCCCGGCC
XM_011545946.2:c.1691-22_1691-21insCCACCGCGCCCGGCC	XP_011544248.1:n.1691-22_1691-21insCCACCGCGCCCGGCC
XM_011545947.2:c.1691-22_1691-21insCCACCGCGCCCGGCC	XP_011544249.1:n.1691-22_1691-21insCCACCGCGCCCGGCC
XM_011545948.2:c.800-22_800-21insCCACCGCGCCCGGCC	XP_011544250.1:n.800-22_800-21insCCACCGCGCCCGGCC
XM_017023671.1:c.1691-22_1691-21insCCACCGCGCCCGGCC	XP_016879160.1:n.1691-22_1691-21insCCACCGCGCCCGGCC
XM_017023672.2:c.1685-22_1685-21insCCACCGCGCCCGGCC	XP_016879161.1:n.1685-22_1685-21insCCACCGCGCCCGGCC
XM_017023673.2:c.1685-22_1685-21insCCACCGCGCCCGGCC	XP_016879162.1:n.1685-22_1685-21insCCACCGCGCCCGGCC
NM_024675.4:c.1685-22_1685-21insCCACCGCGCCCGGCC MANE Select	NP_078951.2:n.1685-22_1685-21insCCACCGCGCCCGGCC