Canonical Allele Identifier: CA2213424641

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630733_23630734delinsAC , CM000678.2:g.23630733_23630734delinsAC	GRCh38
NC_000016.9:g.23642054_23642055delinsAC , CM000678.1:g.23642054_23642055delinsAC	GRCh37
NC_000016.8:g.23549555_23549556delinsAC	NCBI36
NG_007406.1:g.15624_15625delinsGT , LRG_308:g.15624_15625delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-265_1691-264delinsGT	ENSP00000460666.3:n.1691-265_1691-264delinsGT
ENST00000565038.2:c.212-1459_212-1458delinsGT	ENSP00000459882.2:n.212-1459_212-1458delinsGT
ENST00000566069.6:c.1685-265_1685-264delinsGT	ENSP00000459237.2:n.1685-265_1685-264delinsGT
ENST00000697377.2:c.1691-265_1691-264delinsGT	ENSP00000513286.2:n.1691-265_1691-264delinsGT
ENST00000697379.2:c.1691-265_1691-264delinsGT	ENSP00000513287.2:n.1691-265_1691-264delinsGT
ENST00000561514.2:c.800-265_800-264delinsGT	ENSP00000460666.2:n.800-265_800-264delinsGT
ENST00000697374.1:c.800-265_800-264delinsGT	ENSP00000513284.1:n.800-265_800-264delinsGT
ENST00000697375.1:n.3032-265_3032-264delinsGT
ENST00000697376.1:c.800-265_800-264delinsGT	ENSP00000513285.1:n.800-265_800-264delinsGT
ENST00000697377.1:c.800-265_800-264delinsGT	ENSP00000513286.1:n.800-265_800-264delinsGT
ENST00000697378.1:n.2205-265_2205-264delinsGT
ENST00000697379.1:c.800-265_800-264delinsGT	ENSP00000513287.1:n.800-265_800-264delinsGT
ENST00000697380.1:n.348_349delinsGT
ENST00000697381.1:n.364_365delinsGT
ENST00000697382.1:c.800-265_800-264delinsGT	ENSP00000513288.1:n.800-265_800-264delinsGT
ENST00000697383.1:c.49-1459_49-1458delinsGT	ENSP00000513289.1:n.49-1459_49-1458delinsGT
ENST00000697384.1:n.1839-265_1839-264delinsGT
ENST00000261584.9:c.1685-265_1685-264delinsGT MANE Select	ENSP00000261584.4:n.1685-265_1685-264delinsGT
ENST00000261584.8:c.1685-265_1685-264delinsGT	ENSP00000261584.4:n.1685-265_1685-264delinsGT
ENST00000565038.1:c.87-1459_87-1458delinsGT
ENST00000568219.5:c.800-265_800-264delinsGT	ENSP00000454703.2:n.800-265_800-264delinsGT
NM_024675.3:c.1685-265_1685-264delinsGT , LRG_308t1:c.1685-265_1685-264delinsGT	NP_078951.2:n.1685-265_1685-264delinsGT
XM_011545946.1:c.1691-265_1691-264delinsGT	XP_011544248.1:n.1691-265_1691-264delinsGT
XM_011545947.1:c.1691-265_1691-264delinsGT	XP_011544249.1:n.1691-265_1691-264delinsGT
XM_011545948.1:c.800-265_800-264delinsGT	XP_011544250.1:n.800-265_800-264delinsGT
XR_950851.1:n.2481-265_2481-264delinsGT
XM_011545946.2:c.1691-265_1691-264delinsGT	XP_011544248.1:n.1691-265_1691-264delinsGT
XM_011545947.2:c.1691-265_1691-264delinsGT	XP_011544249.1:n.1691-265_1691-264delinsGT
XM_011545948.2:c.800-265_800-264delinsGT	XP_011544250.1:n.800-265_800-264delinsGT
XM_017023671.1:c.1691-265_1691-264delinsGT	XP_016879160.1:n.1691-265_1691-264delinsGT
XM_017023672.2:c.1685-265_1685-264delinsGT	XP_016879161.1:n.1685-265_1685-264delinsGT
XM_017023673.2:c.1685-265_1685-264delinsGT	XP_016879162.1:n.1685-265_1685-264delinsGT
NM_024675.4:c.1685-265_1685-264delinsGT MANE Select	NP_078951.2:n.1685-265_1685-264delinsGT