Canonical Allele Identifier: CA2213424541

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630489_23630492delinsCACA , CM000678.2:g.23630489_23630492delinsCACA	GRCh38
NC_000016.9:g.23641810_23641813delinsCACA , CM000678.1:g.23641810_23641813delinsCACA	GRCh37
NC_000016.8:g.23549311_23549314delinsCACA	NCBI36
NG_007406.1:g.15866_15869delinsTGTG , LRG_308:g.15866_15869delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-23_1691-20delinsTGTG	ENSP00000460666.3:n.1691-23_1691-20delinsTGTG
ENST00000565038.2:c.212-1217_212-1214delinsTGTG	ENSP00000459882.2:n.212-1217_212-1214delinsTGTG
ENST00000566069.6:c.1685-23_1685-20delinsTGTG	ENSP00000459237.2:n.1685-23_1685-20delinsTGTG
ENST00000697377.2:c.1691-23_1691-20delinsTGTG	ENSP00000513286.2:n.1691-23_1691-20delinsTGTG
ENST00000697379.2:c.1691-23_1691-20delinsTGTG	ENSP00000513287.2:n.1691-23_1691-20delinsTGTG
ENST00000561514.2:c.800-23_800-20delinsTGTG	ENSP00000460666.2:n.800-23_800-20delinsTGTG
ENST00000697374.1:c.800-23_800-20delinsTGTG	ENSP00000513284.1:n.800-23_800-20delinsTGTG
ENST00000697375.1:n.3032-23_3032-20delinsTGTG
ENST00000697376.1:c.800-23_800-20delinsTGTG	ENSP00000513285.1:n.800-23_800-20delinsTGTG
ENST00000697377.1:c.800-23_800-20delinsTGTG	ENSP00000513286.1:n.800-23_800-20delinsTGTG
ENST00000697378.1:n.2205-23_2205-20delinsTGTG
ENST00000697379.1:c.800-23_800-20delinsTGTG	ENSP00000513287.1:n.800-23_800-20delinsTGTG
ENST00000697380.1:n.590_593delinsTGTG
ENST00000697381.1:n.380-23_380-20delinsTGTG
ENST00000697382.1:c.800-23_800-20delinsTGTG	ENSP00000513288.1:n.800-23_800-20delinsTGTG
ENST00000697383.1:c.49-1217_49-1214delinsTGTG	ENSP00000513289.1:n.49-1217_49-1214delinsTGTG
ENST00000697384.1:n.1839-23_1839-20delinsTGTG
ENST00000261584.9:c.1685-23_1685-20delinsTGTG MANE Select	ENSP00000261584.4:n.1685-23_1685-20delinsTGTG
ENST00000261584.8:c.1685-23_1685-20delinsTGTG	ENSP00000261584.4:n.1685-23_1685-20delinsTGTG
ENST00000565038.1:c.87-1217_87-1214delinsTGTG
ENST00000568219.5:c.800-23_800-20delinsTGTG	ENSP00000454703.2:n.800-23_800-20delinsTGTG
NM_024675.3:c.1685-23_1685-20delinsTGTG , LRG_308t1:c.1685-23_1685-20delinsTGTG	NP_078951.2:n.1685-23_1685-20delinsTGTG
XM_011545946.1:c.1691-23_1691-20delinsTGTG	XP_011544248.1:n.1691-23_1691-20delinsTGTG
XM_011545947.1:c.1691-23_1691-20delinsTGTG	XP_011544249.1:n.1691-23_1691-20delinsTGTG
XM_011545948.1:c.800-23_800-20delinsTGTG	XP_011544250.1:n.800-23_800-20delinsTGTG
XR_950851.1:n.2481-23_2481-20delinsTGTG
XM_011545946.2:c.1691-23_1691-20delinsTGTG	XP_011544248.1:n.1691-23_1691-20delinsTGTG
XM_011545947.2:c.1691-23_1691-20delinsTGTG	XP_011544249.1:n.1691-23_1691-20delinsTGTG
XM_011545948.2:c.800-23_800-20delinsTGTG	XP_011544250.1:n.800-23_800-20delinsTGTG
XM_017023671.1:c.1691-23_1691-20delinsTGTG	XP_016879160.1:n.1691-23_1691-20delinsTGTG
XM_017023672.2:c.1685-23_1685-20delinsTGTG	XP_016879161.1:n.1685-23_1685-20delinsTGTG
XM_017023673.2:c.1685-23_1685-20delinsTGTG	XP_016879162.1:n.1685-23_1685-20delinsTGTG
NM_024675.4:c.1685-23_1685-20delinsTGTG MANE Select	NP_078951.2:n.1685-23_1685-20delinsTGTG