Canonical Allele Identifier: CA2213420739

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629117_23629123delinsCAAGAAG , CM000678.2:g.23629117_23629123delinsCAAGAAG	GRCh38
NC_000016.9:g.23640438_23640444delinsCAAGAAG , CM000678.1:g.23640438_23640444delinsCAAGAAG	GRCh37
NC_000016.8:g.23547939_23547945delinsCAAGAAG	NCBI36
NG_007406.1:g.17235_17241delinsCTTCTTG , LRG_308:g.17235_17241delinsCTTCTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2592+81_2592+87delinsCTTCTTG	ENSP00000460666.3:n.2592+81_2592+87delins...
ENST00000565038.2:c.*67+81_*67+87delinsCTTCTTG	ENSP00000459882.2:n.*67+81_*67+87delinsCT...
ENST00000566069.6:c.2586+81_2586+87delinsCTTCTTG	ENSP00000459237.2:n.2586+81_2586+87delins...
ENST00000697377.2:c.2592+81_2592+87delinsCTTCTTG	ENSP00000513286.2:n.2592+81_2592+87delins...
ENST00000697379.2:c.2592+81_2592+87delinsCTTCTTG	ENSP00000513287.2:n.2592+81_2592+87delins...
ENST00000561514.2:c.1701+81_1701+87delinsCTTCTTG	ENSP00000460666.2:n.1701+81_1701+87delins...
ENST00000697374.1:c.1701+81_1701+87delinsCTTCTTG	ENSP00000513284.1:n.1701+81_1701+87delins...
ENST00000697375.1:n.3933+81_3933+87delinsCTTCTTG
ENST00000697376.1:c.1701+81_1701+87delinsCTTCTTG	ENSP00000513285.1:n.1701+81_1701+87delins...
ENST00000697377.1:c.1701+81_1701+87delinsCTTCTTG	ENSP00000513286.1:n.1701+81_1701+87delins...
ENST00000697378.1:n.3106+81_3106+87delinsCTTCTTG
ENST00000697379.1:c.1701+81_1701+87delinsCTTCTTG	ENSP00000513287.1:n.1701+81_1701+87delins...
ENST00000697380.1:n.1878+81_1878+87delinsCTTCTTG
ENST00000697381.1:n.1281+81_1281+87delinsCTTCTTG
ENST00000697382.1:c.1701+81_1701+87delinsCTTCTTG	ENSP00000513288.1:n.1701+81_1701+87delins...
ENST00000697383.1:c.120+81_120+87delinsCTTCTTG	ENSP00000513289.1:n.120+81_120+87delinsCT...
ENST00000697384.1:n.2821_2827delinsCTTCTTG
ENST00000261584.9:c.2586+81_2586+87delinsCTTCTTG MANE Select	ENSP00000261584.4:n.2586+81_2586+87delins...
ENST00000261584.8:c.2586+81_2586+87delinsCTTCTTG	ENSP00000261584.4:n.2586+81_2586+87delins...
ENST00000565038.1:c.158+81_158+87delinsCTTCTTG
ENST00000568219.5:c.1701+81_1701+87delinsCTTCTTG	ENSP00000454703.2:n.1701+81_1701+87delins...
NM_024675.3:c.2586+81_2586+87delinsCTTCTTG , LRG_308t1:c.2586+81_2586+87delinsCTTCTTG	NP_078951.2:n.2586+81_2586+87delinsCTTCTT...
XM_011545946.1:c.2592+81_2592+87delinsCTTCTTG	XP_011544248.1:n.2592+81_2592+87delinsCTT...
XM_011545947.1:c.2592+81_2592+87delinsCTTCTTG	XP_011544249.1:n.2592+81_2592+87delinsCTT...
XM_011545948.1:c.1701+81_1701+87delinsCTTCTTG	XP_011544250.1:n.1701+81_1701+87delinsCTT...
XR_950851.1:n.3382+81_3382+87delinsCTTCTTG
XM_011545946.2:c.2592+81_2592+87delinsCTTCTTG	XP_011544248.1:n.2592+81_2592+87delinsCTT...
XM_011545947.2:c.2592+81_2592+87delinsCTTCTTG	XP_011544249.1:n.2592+81_2592+87delinsCTT...
XM_011545948.2:c.1701+81_1701+87delinsCTTCTTG	XP_011544250.1:n.1701+81_1701+87delinsCTT...
XM_017023671.1:c.2592+81_2592+87delinsCTTCTTG	XP_016879160.1:n.2592+81_2592+87delinsCTT...
XM_017023672.2:c.2586+81_2586+87delinsCTTCTTG	XP_016879161.1:n.2586+81_2586+87delinsCTT...
XM_017023673.2:c.2586+81_2586+87delinsCTTCTTG	XP_016879162.1:n.2586+81_2586+87delinsCTT...
NM_024675.4:c.2586+81_2586+87delinsCTTCTTG MANE Select	NP_078951.2:n.2586+81_2586+87delinsCTTCTT...