Canonical Allele Identifier: CA2213412037

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23622959_23622960delinsCT , CM000678.2:g.23622959_23622960delinsCT	GRCh38
NC_000016.9:g.23634280_23634281delinsCT , CM000678.1:g.23634280_23634281delinsCT	GRCh37
NC_000016.8:g.23541781_23541782delinsCT	NCBI36
NG_007406.1:g.23398_23399delinsAG , LRG_308:g.23398_23399delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3002+9_3002+10delinsAG	ENSP00000460666.3:n.3002+9_3002+10delinsAG
ENST00000565038.2:c.*477+9_*477+10delinsAG	ENSP00000459882.2:n.*477+9_*477+10delinsAG
ENST00000566069.6:c.2996+9_2996+10delinsAG	ENSP00000459237.2:n.2996+9_2996+10delinsAG
ENST00000697377.2:c.2840+9_2840+10delinsAG	ENSP00000513286.2:n.2840+9_2840+10delinsAG
ENST00000697379.2:c.3002+9_3002+10delinsAG	ENSP00000513287.2:n.3002+9_3002+10delinsAG
ENST00000561514.2:c.2111+9_2111+10delinsAG	ENSP00000460666.2:n.2111+9_2111+10delinsAG
ENST00000697374.1:c.2111+9_2111+10delinsAG	ENSP00000513284.1:n.2111+9_2111+10delinsAG
ENST00000697375.1:n.4343+9_4343+10delinsAG
ENST00000697376.1:c.2111+9_2111+10delinsAG	ENSP00000513285.1:n.2111+9_2111+10delinsAG
ENST00000697377.1:c.1949+9_1949+10delinsAG	ENSP00000513286.1:n.1949+9_1949+10delinsAG
ENST00000697378.1:n.3516+9_3516+10delinsAG
ENST00000697379.1:c.2111+9_2111+10delinsAG	ENSP00000513287.1:n.2111+9_2111+10delinsAG
ENST00000697380.1:n.2288+9_2288+10delinsAG
ENST00000697381.1:n.1691+9_1691+10delinsAG
ENST00000697382.1:c.2111+9_2111+10delinsAG	ENSP00000513288.1:n.2111+9_2111+10delinsAG
ENST00000697383.1:c.530+9_530+10delinsAG	ENSP00000513289.1:n.530+9_530+10delinsAG
ENST00000261584.9:c.2996+9_2996+10delinsAG MANE Select	ENSP00000261584.4:n.2996+9_2996+10delinsAG
ENST00000261584.8:c.2996+9_2996+10delinsAG	ENSP00000261584.4:n.2996+9_2996+10delinsAG
ENST00000568219.5:c.2111+9_2111+10delinsAG	ENSP00000454703.2:n.2111+9_2111+10delinsAG
NM_024675.3:c.2996+9_2996+10delinsAG , LRG_308t1:c.2996+9_2996+10delinsAG	NP_078951.2:n.2996+9_2996+10delinsAG
XM_011545946.1:c.3002+9_3002+10delinsAG	XP_011544248.1:n.3002+9_3002+10delinsAG
XM_011545947.1:c.3002+9_3002+10delinsAG	XP_011544249.1:n.3002+9_3002+10delinsAG
XM_011545948.1:c.2111+9_2111+10delinsAG	XP_011544250.1:n.2111+9_2111+10delinsAG
XR_950851.1:n.3792+9_3792+10delinsAG
XM_011545946.2:c.3002+9_3002+10delinsAG	XP_011544248.1:n.3002+9_3002+10delinsAG
XM_011545947.2:c.3002+9_3002+10delinsAG	XP_011544249.1:n.3002+9_3002+10delinsAG
XM_011545948.2:c.2111+9_2111+10delinsAG	XP_011544250.1:n.2111+9_2111+10delinsAG
XM_017023671.1:c.3002+9_3002+10delinsAG	XP_016879160.1:n.3002+9_3002+10delinsAG
XM_017023672.2:c.2996+9_2996+10delinsAG	XP_016879161.1:n.2996+9_2996+10delinsAG
XM_017023673.2:c.2996+9_2996+10delinsAG	XP_016879162.1:n.2996+9_2996+10delinsAG
NM_024675.4:c.2996+9_2996+10delinsAG MANE Select	NP_078951.2:n.2996+9_2996+10delinsAG