Canonical Allele Identifier: CA2213431885

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636101_23636102delinsTC , CM000678.2:g.23636101_23636102delinsTC	GRCh38
NC_000016.9:g.23647422_23647423delinsTC , CM000678.1:g.23647422_23647423delinsTC	GRCh37
NC_000016.8:g.23554923_23554924delinsTC	NCBI36
NG_007406.1:g.10256_10257delinsGA , LRG_308:g.10256_10257delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.450_451delinsGA	ENSP00000460666.3:p.Lys150=
ENST00000565038.2:c.211+1748_211+1749delinsGA	ENSP00000459882.2:n.211+1748_211+1749delinsGA
ENST00000566069.6:c.444_445delinsGA	ENSP00000459237.2:p.Lys148=
ENST00000697377.2:c.450_451delinsGA	ENSP00000513286.2:p.Lys150=
ENST00000697379.2:c.450_451delinsGA	ENSP00000513287.2:p.Lys150=
ENST00000561514.2:c.-442_-441delinsGA	ENSP00000460666.2:n.-442_-441delinsGA
ENST00000697374.1:c.-442_-441delinsGA	ENSP00000513284.1:n.-442_-441delinsGA
ENST00000697375.1:n.1791_1792delinsGA
ENST00000697376.1:c.-442_-441delinsGA	ENSP00000513285.1:n.-442_-441delinsGA
ENST00000697377.1:c.-442_-441delinsGA	ENSP00000513286.1:n.-442_-441delinsGA
ENST00000697378.1:n.964_965delinsGA
ENST00000697379.1:c.-442_-441delinsGA	ENSP00000513287.1:n.-442_-441delinsGA
ENST00000697382.1:c.-442_-441delinsGA	ENSP00000513288.1:n.-442_-441delinsGA
ENST00000697383.1:c.48+5008_48+5009delinsGA	ENSP00000513289.1:n.48+5008_48+5009delinsGA
ENST00000697384.1:n.598_599delinsGA
ENST00000261584.9:c.444_445delinsGA MANE Select	ENSP00000261584.4:p.Lys148=
ENST00000261584.8:c.444_445delinsGA	ENSP00000261584.4:p.Lys148=
ENST00000565038.1:c.86+1748_86+1749delinsGA
ENST00000567003.1:n.722_723delinsGA
ENST00000568219.5:c.-442_-441delinsGA	ENSP00000454703.2:n.-442_-441delinsGA
NM_024675.3:c.444_445delinsGA , LRG_308t1:c.444_445delinsGA	NP_078951.2:p.Lys148=
XM_011545946.1:c.450_451delinsGA	XP_011544248.1:p.Lys150=
XM_011545947.1:c.450_451delinsGA	XP_011544249.1:p.Lys150=
XM_011545948.1:c.-442_-441delinsGA	XP_011544250.1:n.-442_-441delinsGA
XR_950851.1:n.1240_1241delinsGA
XM_011545946.2:c.450_451delinsGA	XP_011544248.1:p.Lys150=
XM_011545947.2:c.450_451delinsGA	XP_011544249.1:p.Lys150=
XM_011545948.2:c.-442_-441delinsGA	XP_011544250.1:n.-442_-441delinsGA
XM_017023671.1:c.450_451delinsGA	XP_016879160.1:p.Lys150=
XM_017023672.2:c.444_445delinsGA	XP_016879161.1:p.Lys148=
XM_017023673.2:c.444_445delinsGA	XP_016879162.1:p.Lys148=
NM_024675.4:c.444_445delinsGA MANE Select	NP_078951.2:p.Lys148=