Canonical Allele Identifier: CA2806270554

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630505_23630506insCCACACCAAACAC , CM000678.2:g.23630505_23630506insCCACACCAAACAC	GRCh38
NC_000016.9:g.23641826_23641827insCCACACCAAACAC , CM000678.1:g.23641826_23641827insCCACACCAAACAC	GRCh37
NC_000016.8:g.23549327_23549328insCCACACCAAACAC	NCBI36
NG_007406.1:g.15852_15853insGTGTTTGGTGTGG , LRG_308:g.15852_15853insGTGTTTGGTGTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-37_1691-36insGTGTTTGGTGTGG	ENSP00000460666.3:n.1691-37_1691-36insGTGTTTGGTGTGG
ENST00000565038.2:c.212-1231_212-1230insGTGTTTGGTGTGG	ENSP00000459882.2:n.212-1231_212-1230insGTGTTTGGTGTGG
ENST00000566069.6:c.1685-37_1685-36insGTGTTTGGTGTGG	ENSP00000459237.2:n.1685-37_1685-36insGTGTTTGGTGTGG
ENST00000697377.2:c.1691-37_1691-36insGTGTTTGGTGTGG	ENSP00000513286.2:n.1691-37_1691-36insGTGTTTGGTGTGG
ENST00000697379.2:c.1691-37_1691-36insGTGTTTGGTGTGG	ENSP00000513287.2:n.1691-37_1691-36insGTGTTTGGTGTGG
ENST00000561514.2:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000460666.2:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697374.1:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000513284.1:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697375.1:n.3032-37_3032-36insGTGTTTGGTGTGG
ENST00000697376.1:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000513285.1:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697377.1:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000513286.1:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697378.1:n.2205-37_2205-36insGTGTTTGGTGTGG
ENST00000697379.1:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000513287.1:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697380.1:n.576_577insGTGTTTGGTGTGG
ENST00000697381.1:n.380-37_380-36insGTGTTTGGTGTGG
ENST00000697382.1:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000513288.1:n.800-37_800-36insGTGTTTGGTGTGG
ENST00000697383.1:c.49-1231_49-1230insGTGTTTGGTGTGG	ENSP00000513289.1:n.49-1231_49-1230insGTGTTTGGTGTGG
ENST00000697384.1:n.1839-37_1839-36insGTGTTTGGTGTGG
ENST00000261584.9:c.1685-37_1685-36insGTGTTTGGTGTGG MANE Select	ENSP00000261584.4:n.1685-37_1685-36insGTGTTTGGTGTGG
ENST00000261584.8:c.1685-37_1685-36insGTGTTTGGTGTGG	ENSP00000261584.4:n.1685-37_1685-36insGTGTTTGGTGTGG
ENST00000565038.1:c.87-1231_87-1230insGTGTTTGGTGTGG
ENST00000568219.5:c.800-37_800-36insGTGTTTGGTGTGG	ENSP00000454703.2:n.800-37_800-36insGTGTTTGGTGTGG
NM_024675.3:c.1685-37_1685-36insGTGTTTGGTGTGG , LRG_308t1:c.1685-37_1685-36insGTGTTTGGTGTGG	NP_078951.2:n.1685-37_1685-36insGTGTTTGGTGTGG
XM_011545946.1:c.1691-37_1691-36insGTGTTTGGTGTGG	XP_011544248.1:n.1691-37_1691-36insGTGTTTGGTGTGG
XM_011545947.1:c.1691-37_1691-36insGTGTTTGGTGTGG	XP_011544249.1:n.1691-37_1691-36insGTGTTTGGTGTGG
XM_011545948.1:c.800-37_800-36insGTGTTTGGTGTGG	XP_011544250.1:n.800-37_800-36insGTGTTTGGTGTGG
XR_950851.1:n.2481-37_2481-36insGTGTTTGGTGTGG
XM_011545946.2:c.1691-37_1691-36insGTGTTTGGTGTGG	XP_011544248.1:n.1691-37_1691-36insGTGTTTGGTGTGG
XM_011545947.2:c.1691-37_1691-36insGTGTTTGGTGTGG	XP_011544249.1:n.1691-37_1691-36insGTGTTTGGTGTGG
XM_011545948.2:c.800-37_800-36insGTGTTTGGTGTGG	XP_011544250.1:n.800-37_800-36insGTGTTTGGTGTGG
XM_017023671.1:c.1691-37_1691-36insGTGTTTGGTGTGG	XP_016879160.1:n.1691-37_1691-36insGTGTTTGGTGTGG
XM_017023672.2:c.1685-37_1685-36insGTGTTTGGTGTGG	XP_016879161.1:n.1685-37_1685-36insGTGTTTGGTGTGG
XM_017023673.2:c.1685-37_1685-36insGTGTTTGGTGTGG	XP_016879162.1:n.1685-37_1685-36insGTGTTTGGTGTGG
NM_024675.4:c.1685-37_1685-36insGTGTTTGGTGTGG MANE Select	NP_078951.2:n.1685-37_1685-36insGTGTTTGGTGTGG