Canonical Allele Identifier: CA2213429176

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635422_23635426delinsAGAAT , CM000678.2:g.23635422_23635426delinsAGAAT	GRCh38
NC_000016.9:g.23646743_23646747delinsAGAAT , CM000678.1:g.23646743_23646747delinsAGAAT	GRCh37
NC_000016.8:g.23554244_23554248delinsAGAAT	NCBI36
NG_007406.1:g.10932_10936delinsATTCT , LRG_308:g.10932_10936delinsATTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1126_1130delinsATTCT	ENSP00000460666.3:p.Ile376=
ENST00000565038.2:c.211+2424_211+2428delinsATTCT	ENSP00000459882.2:n.211+2424_211+2428delinsATTCT
ENST00000566069.6:c.1120_1124delinsATTCT	ENSP00000459237.2:p.Ile374=
ENST00000697377.2:c.1126_1130delinsATTCT	ENSP00000513286.2:p.Ile376=
ENST00000697379.2:c.1126_1130delinsATTCT	ENSP00000513287.2:p.Ile376=
ENST00000561514.2:c.235_239delinsATTCT	ENSP00000460666.2:p.Ile79=
ENST00000697374.1:c.235_239delinsATTCT	ENSP00000513284.1:p.Ile79=
ENST00000697375.1:n.2467_2471delinsATTCT
ENST00000697376.1:c.235_239delinsATTCT	ENSP00000513285.1:p.Ile79=
ENST00000697377.1:c.235_239delinsATTCT	ENSP00000513286.1:p.Ile79=
ENST00000697378.1:n.1640_1644delinsATTCT
ENST00000697379.1:c.235_239delinsATTCT	ENSP00000513287.1:p.Ile79=
ENST00000697382.1:c.235_239delinsATTCT	ENSP00000513288.1:p.Ile79=
ENST00000697383.1:c.48+5684_48+5688delinsATTCT	ENSP00000513289.1:n.48+5684_48+5688delinsATTCT
ENST00000697384.1:n.1274_1278delinsATTCT
ENST00000261584.9:c.1120_1124delinsATTCT MANE Select	ENSP00000261584.4:p.Ile374=
ENST00000261584.8:c.1120_1124delinsATTCT	ENSP00000261584.4:p.Ile374=
ENST00000565038.1:c.86+2424_86+2428delinsATTCT
ENST00000568219.5:c.235_239delinsATTCT	ENSP00000454703.2:p.Ile79=
NM_024675.3:c.1120_1124delinsATTCT , LRG_308t1:c.1120_1124delinsATTCT	NP_078951.2:p.Ile374=
XM_011545946.1:c.1126_1130delinsATTCT	XP_011544248.1:p.Ile376=
XM_011545947.1:c.1126_1130delinsATTCT	XP_011544249.1:p.Ile376=
XM_011545948.1:c.235_239delinsATTCT	XP_011544250.1:p.Ile79=
XR_950851.1:n.1916_1920delinsATTCT
XM_011545946.2:c.1126_1130delinsATTCT	XP_011544248.1:p.Ile376=
XM_011545947.2:c.1126_1130delinsATTCT	XP_011544249.1:p.Ile376=
XM_011545948.2:c.235_239delinsATTCT	XP_011544250.1:p.Ile79=
XM_017023671.1:c.1126_1130delinsATTCT	XP_016879160.1:p.Ile376=
XM_017023672.2:c.1120_1124delinsATTCT	XP_016879161.1:p.Ile374=
XM_017023673.2:c.1120_1124delinsATTCT	XP_016879162.1:p.Ile374=
NM_024675.4:c.1120_1124delinsATTCT MANE Select	NP_078951.2:p.Ile374=