Canonical Allele Identifier: CA2806270557

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630557_23630561del , CM000678.2:g.23630557_23630561del	GRCh38
NC_000016.9:g.23641878_23641882del , CM000678.1:g.23641878_23641882del	GRCh37
NC_000016.8:g.23549379_23549383del	NCBI36
NG_007406.1:g.15797_15801del , LRG_308:g.15797_15801del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-92_1691-88del	ENSP00000460666.3:n.1691-92_1691-88del
ENST00000565038.2:c.212-1286_212-1282del	ENSP00000459882.2:n.212-1286_212-1282del
ENST00000566069.6:c.1685-92_1685-88del	ENSP00000459237.2:n.1685-92_1685-88del
ENST00000697377.2:c.1691-92_1691-88del	ENSP00000513286.2:n.1691-92_1691-88del
ENST00000697379.2:c.1691-92_1691-88del	ENSP00000513287.2:n.1691-92_1691-88del
ENST00000561514.2:c.800-92_800-88del	ENSP00000460666.2:n.800-92_800-88del
ENST00000697374.1:c.800-92_800-88del	ENSP00000513284.1:n.800-92_800-88del
ENST00000697375.1:n.3032-92_3032-88del
ENST00000697376.1:c.800-92_800-88del	ENSP00000513285.1:n.800-92_800-88del
ENST00000697377.1:c.800-92_800-88del	ENSP00000513286.1:n.800-92_800-88del
ENST00000697378.1:n.2205-92_2205-88del
ENST00000697379.1:c.800-92_800-88del	ENSP00000513287.1:n.800-92_800-88del
ENST00000697380.1:n.521_525del
ENST00000697381.1:n.380-92_380-88del
ENST00000697382.1:c.800-92_800-88del	ENSP00000513288.1:n.800-92_800-88del
ENST00000697383.1:c.49-1286_49-1282del	ENSP00000513289.1:n.49-1286_49-1282del
ENST00000697384.1:n.1839-92_1839-88del
ENST00000261584.9:c.1685-92_1685-88del MANE Select	ENSP00000261584.4:n.1685-92_1685-88del
ENST00000261584.8:c.1685-92_1685-88del	ENSP00000261584.4:n.1685-92_1685-88del
ENST00000565038.1:c.87-1286_87-1282del
ENST00000568219.5:c.800-92_800-88del	ENSP00000454703.2:n.800-92_800-88del
NM_024675.3:c.1685-92_1685-88del , LRG_308t1:c.1685-92_1685-88del	NP_078951.2:n.1685-92_1685-88del
XM_011545946.1:c.1691-92_1691-88del	XP_011544248.1:n.1691-92_1691-88del
XM_011545947.1:c.1691-92_1691-88del	XP_011544249.1:n.1691-92_1691-88del
XM_011545948.1:c.800-92_800-88del	XP_011544250.1:n.800-92_800-88del
XR_950851.1:n.2481-92_2481-88del
XM_011545946.2:c.1691-92_1691-88del	XP_011544248.1:n.1691-92_1691-88del
XM_011545947.2:c.1691-92_1691-88del	XP_011544249.1:n.1691-92_1691-88del
XM_011545948.2:c.800-92_800-88del	XP_011544250.1:n.800-92_800-88del
XM_017023671.1:c.1691-92_1691-88del	XP_016879160.1:n.1691-92_1691-88del
XM_017023672.2:c.1685-92_1685-88del	XP_016879161.1:n.1685-92_1685-88del
XM_017023673.2:c.1685-92_1685-88del	XP_016879162.1:n.1685-92_1685-88del
NM_024675.4:c.1685-92_1685-88del MANE Select	NP_078951.2:n.1685-92_1685-88del