Canonical Allele Identifier: CA2213424655

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630760_23630761delinsAC , CM000678.2:g.23630760_23630761delinsAC	GRCh38
NC_000016.9:g.23642081_23642082delinsAC , CM000678.1:g.23642081_23642082delinsAC	GRCh37
NC_000016.8:g.23549582_23549583delinsAC	NCBI36
NG_007406.1:g.15597_15598delinsGT , LRG_308:g.15597_15598delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-292_1691-291delinsGT	ENSP00000460666.3:n.1691-292_1691-291delinsGT
ENST00000565038.2:c.212-1486_212-1485delinsGT	ENSP00000459882.2:n.212-1486_212-1485delinsGT
ENST00000566069.6:c.1685-292_1685-291delinsGT	ENSP00000459237.2:n.1685-292_1685-291delinsGT
ENST00000697377.2:c.1691-292_1691-291delinsGT	ENSP00000513286.2:n.1691-292_1691-291delinsGT
ENST00000697379.2:c.1691-292_1691-291delinsGT	ENSP00000513287.2:n.1691-292_1691-291delinsGT
ENST00000561514.2:c.800-292_800-291delinsGT	ENSP00000460666.2:n.800-292_800-291delinsGT
ENST00000697374.1:c.800-292_800-291delinsGT	ENSP00000513284.1:n.800-292_800-291delinsGT
ENST00000697375.1:n.3032-292_3032-291delinsGT
ENST00000697376.1:c.800-292_800-291delinsGT	ENSP00000513285.1:n.800-292_800-291delinsGT
ENST00000697377.1:c.800-292_800-291delinsGT	ENSP00000513286.1:n.800-292_800-291delinsGT
ENST00000697378.1:n.2205-292_2205-291delinsGT
ENST00000697379.1:c.800-292_800-291delinsGT	ENSP00000513287.1:n.800-292_800-291delinsGT
ENST00000697380.1:n.321_322delinsGT
ENST00000697381.1:n.337_338delinsGT
ENST00000697382.1:c.800-292_800-291delinsGT	ENSP00000513288.1:n.800-292_800-291delinsGT
ENST00000697383.1:c.49-1486_49-1485delinsGT	ENSP00000513289.1:n.49-1486_49-1485delinsGT
ENST00000697384.1:n.1839-292_1839-291delinsGT
ENST00000261584.9:c.1685-292_1685-291delinsGT MANE Select	ENSP00000261584.4:n.1685-292_1685-291delinsGT
ENST00000261584.8:c.1685-292_1685-291delinsGT	ENSP00000261584.4:n.1685-292_1685-291delinsGT
ENST00000565038.1:c.87-1486_87-1485delinsGT
ENST00000568219.5:c.800-292_800-291delinsGT	ENSP00000454703.2:n.800-292_800-291delinsGT
NM_024675.3:c.1685-292_1685-291delinsGT , LRG_308t1:c.1685-292_1685-291delinsGT	NP_078951.2:n.1685-292_1685-291delinsGT
XM_011545946.1:c.1691-292_1691-291delinsGT	XP_011544248.1:n.1691-292_1691-291delinsGT
XM_011545947.1:c.1691-292_1691-291delinsGT	XP_011544249.1:n.1691-292_1691-291delinsGT
XM_011545948.1:c.800-292_800-291delinsGT	XP_011544250.1:n.800-292_800-291delinsGT
XR_950851.1:n.2481-292_2481-291delinsGT
XM_011545946.2:c.1691-292_1691-291delinsGT	XP_011544248.1:n.1691-292_1691-291delinsGT
XM_011545947.2:c.1691-292_1691-291delinsGT	XP_011544249.1:n.1691-292_1691-291delinsGT
XM_011545948.2:c.800-292_800-291delinsGT	XP_011544250.1:n.800-292_800-291delinsGT
XM_017023671.1:c.1691-292_1691-291delinsGT	XP_016879160.1:n.1691-292_1691-291delinsGT
XM_017023672.2:c.1685-292_1685-291delinsGT	XP_016879161.1:n.1685-292_1685-291delinsGT
XM_017023673.2:c.1685-292_1685-291delinsGT	XP_016879162.1:n.1685-292_1685-291delinsGT
NM_024675.4:c.1685-292_1685-291delinsGT MANE Select	NP_078951.2:n.1685-292_1685-291delinsGT