Canonical Allele Identifier: CA2213424555

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630515_23630519delinsAACAG , CM000678.2:g.23630515_23630519delinsAACAG	GRCh38
NC_000016.9:g.23641836_23641840delinsAACAG , CM000678.1:g.23641836_23641840delinsAACAG	GRCh37
NC_000016.8:g.23549337_23549341delinsAACAG	NCBI36
NG_007406.1:g.15839_15843delinsCTGTT , LRG_308:g.15839_15843delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-50_1691-46delinsCTGTT	ENSP00000460666.3:n.1691-50_1691-46delinsCTGTT
ENST00000565038.2:c.212-1244_212-1240delinsCTGTT	ENSP00000459882.2:n.212-1244_212-1240delinsCTGTT
ENST00000566069.6:c.1685-50_1685-46delinsCTGTT	ENSP00000459237.2:n.1685-50_1685-46delinsCTGTT
ENST00000697377.2:c.1691-50_1691-46delinsCTGTT	ENSP00000513286.2:n.1691-50_1691-46delinsCTGTT
ENST00000697379.2:c.1691-50_1691-46delinsCTGTT	ENSP00000513287.2:n.1691-50_1691-46delinsCTGTT
ENST00000561514.2:c.800-50_800-46delinsCTGTT	ENSP00000460666.2:n.800-50_800-46delinsCTGTT
ENST00000697374.1:c.800-50_800-46delinsCTGTT	ENSP00000513284.1:n.800-50_800-46delinsCTGTT
ENST00000697375.1:n.3032-50_3032-46delinsCTGTT
ENST00000697376.1:c.800-50_800-46delinsCTGTT	ENSP00000513285.1:n.800-50_800-46delinsCTGTT
ENST00000697377.1:c.800-50_800-46delinsCTGTT	ENSP00000513286.1:n.800-50_800-46delinsCTGTT
ENST00000697378.1:n.2205-50_2205-46delinsCTGTT
ENST00000697379.1:c.800-50_800-46delinsCTGTT	ENSP00000513287.1:n.800-50_800-46delinsCTGTT
ENST00000697380.1:n.563_567delinsCTGTT
ENST00000697381.1:n.380-50_380-46delinsCTGTT
ENST00000697382.1:c.800-50_800-46delinsCTGTT	ENSP00000513288.1:n.800-50_800-46delinsCTGTT
ENST00000697383.1:c.49-1244_49-1240delinsCTGTT	ENSP00000513289.1:n.49-1244_49-1240delinsCTGTT
ENST00000697384.1:n.1839-50_1839-46delinsCTGTT
ENST00000261584.9:c.1685-50_1685-46delinsCTGTT MANE Select	ENSP00000261584.4:n.1685-50_1685-46delinsCTGTT
ENST00000261584.8:c.1685-50_1685-46delinsCTGTT	ENSP00000261584.4:n.1685-50_1685-46delinsCTGTT
ENST00000565038.1:c.87-1244_87-1240delinsCTGTT
ENST00000568219.5:c.800-50_800-46delinsCTGTT	ENSP00000454703.2:n.800-50_800-46delinsCTGTT
NM_024675.3:c.1685-50_1685-46delinsCTGTT , LRG_308t1:c.1685-50_1685-46delinsCTGTT	NP_078951.2:n.1685-50_1685-46delinsCTGTT
XM_011545946.1:c.1691-50_1691-46delinsCTGTT	XP_011544248.1:n.1691-50_1691-46delinsCTGTT
XM_011545947.1:c.1691-50_1691-46delinsCTGTT	XP_011544249.1:n.1691-50_1691-46delinsCTGTT
XM_011545948.1:c.800-50_800-46delinsCTGTT	XP_011544250.1:n.800-50_800-46delinsCTGTT
XR_950851.1:n.2481-50_2481-46delinsCTGTT
XM_011545946.2:c.1691-50_1691-46delinsCTGTT	XP_011544248.1:n.1691-50_1691-46delinsCTGTT
XM_011545947.2:c.1691-50_1691-46delinsCTGTT	XP_011544249.1:n.1691-50_1691-46delinsCTGTT
XM_011545948.2:c.800-50_800-46delinsCTGTT	XP_011544250.1:n.800-50_800-46delinsCTGTT
XM_017023671.1:c.1691-50_1691-46delinsCTGTT	XP_016879160.1:n.1691-50_1691-46delinsCTGTT
XM_017023672.2:c.1685-50_1685-46delinsCTGTT	XP_016879161.1:n.1685-50_1685-46delinsCTGTT
XM_017023673.2:c.1685-50_1685-46delinsCTGTT	XP_016879162.1:n.1685-50_1685-46delinsCTGTT
NM_024675.4:c.1685-50_1685-46delinsCTGTT MANE Select	NP_078951.2:n.1685-50_1685-46delinsCTGTT