Canonical Allele Identifier: CA2213428784

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607903_23607919delinsCCCACGCTGAGAGTCGT , CM000678.2:g.23607903_23607919delinsCCCACGCTGAGAGTCGT	GRCh38
NC_000016.9:g.23619224_23619240delinsCCCACGCTGAGAGTCGT , CM000678.1:g.23619224_23619240delinsCCCACGCTGAGAGTCGT	GRCh37
NC_000016.8:g.23526725_23526741delinsCCCACGCTGAGAGTCGT	NCBI36
NG_007406.1:g.38439_38455delinsACGACTCTCAGCGTGGG , LRG_308:g.38439_38455delinsACGACTCTCAGCGTGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3301_3317delinsACGACTCTCAGCGTGGG	ENSP00000460666.3:p.Thr1101=
ENST00000565038.2:c.*776_*792delinsACGACTCTCAGCGTGGG	ENSP00000459882.2:n.*776_*792delinsACGACT...
ENST00000566069.6:c.3202-4250_3202-4234delinsACGACTCTCAGCGTGGG	ENSP00000459237.2:n.3202-4250_3202-4234de...
ENST00000697377.2:c.3139_3155delinsACGACTCTCAGCGTGGG	ENSP00000513286.2:p.Thr1047=
ENST00000697379.2:c.3301_3317delinsACGACTCTCAGCGTGGG	ENSP00000513287.2:p.Thr1101=
ENST00000561514.2:c.2410_2426delinsACGACTCTCAGCGTGGG	ENSP00000460666.2:p.Thr804=
ENST00000697374.1:c.2410_2426delinsACGACTCTCAGCGTGGG	ENSP00000513284.1:p.Thr804=
ENST00000697375.1:n.4642_4658delinsACGACTCTCAGCGTGGG
ENST00000697376.1:c.2317-4250_2317-4234delinsACGACTCTCAGCGTGGG	ENSP00000513285.1:n.2317-4250_2317-4234de...
ENST00000697377.1:c.2248_2264delinsACGACTCTCAGCGTGGG	ENSP00000513286.1:p.Thr750=
ENST00000697378.1:n.3815_3831delinsACGACTCTCAGCGTGGG
ENST00000697379.1:c.2410_2426delinsACGACTCTCAGCGTGGG	ENSP00000513287.1:p.Thr804=
ENST00000697380.1:n.2499_2515delinsACGACTCTCAGCGTGGG
ENST00000697381.1:n.1990_2006delinsACGACTCTCAGCGTGGG
ENST00000697382.1:c.*72_*88delinsACGACTCTCAGCGTGGG	ENSP00000513288.1:n.*72_*88delinsACGACTCT...
ENST00000697383.1:c.829_845delinsACGACTCTCAGCGTGGG	ENSP00000513289.1:p.Thr277=
ENST00000261584.9:c.3295_3311delinsACGACTCTCAGCGTGGG MANE Select	ENSP00000261584.4:p.Thr1099=
ENST00000261584.8:c.3295_3311delinsACGACTCTCAGCGTGGG	ENSP00000261584.4:p.Thr1099=
ENST00000566069.5:c.117-4250_117-4234delinsACGACTCTCAGCGTGGG
ENST00000568219.5:c.2410_2426delinsACGACTCTCAGCGTGGG	ENSP00000454703.2:p.Thr804=
NM_024675.3:c.3295_3311delinsACGACTCTCAGCGTGGG , LRG_308t1:c.3295_3311delinsACGACTCTCAGCGTGGG	NP_078951.2:p.Thr1099=
XM_011545946.1:c.3301_3317delinsACGACTCTCAGCGTGGG	XP_011544248.1:p.Thr1101=
XM_011545947.1:c.3208-4250_3208-4234delinsACGACTCTCAGCGTGGG	XP_011544249.1:n.3208-4250_3208-4234delin...
XM_011545948.1:c.2410_2426delinsACGACTCTCAGCGTGGG	XP_011544250.1:p.Thr804=
XR_950851.1:n.4003_4019delinsACGACTCTCAGCGTGGG
XM_011545946.2:c.3301_3317delinsACGACTCTCAGCGTGGG	XP_011544248.1:p.Thr1101=
XM_011545947.2:c.3208-4250_3208-4234delinsACGACTCTCAGCGTGGG	XP_011544249.1:n.3208-4250_3208-4234delin...
XM_011545948.2:c.2410_2426delinsACGACTCTCAGCGTGGG	XP_011544250.1:p.Thr804=
XM_017023671.1:c.3120-4250_3120-4234delinsACGACTCTCAGCGTGGG	XP_016879160.1:n.3120-4250_3120-4234delin...
XM_017023672.2:c.3114-4250_3114-4234delinsACGACTCTCAGCGTGGG	XP_016879161.1:n.3114-4250_3114-4234delin...
XM_017023673.2:c.3202-4250_3202-4234delinsACGACTCTCAGCGTGGG	XP_016879162.1:n.3202-4250_3202-4234delin...
NM_024675.4:c.3295_3311delinsACGACTCTCAGCGTGGG MANE Select	NP_078951.2:p.Thr1099=