Canonical Allele Identifier: CA2213428815

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607917_23607918delinsCG , CM000678.2:g.23607917_23607918delinsCG	GRCh38
NC_000016.9:g.23619238_23619239delinsCG , CM000678.1:g.23619238_23619239delinsCG	GRCh37
NC_000016.8:g.23526739_23526740delinsCG	NCBI36
NG_007406.1:g.38440_38441delinsCG , LRG_308:g.38440_38441delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3302_3303delinsCG	ENSP00000460666.3:p.Thr1101=
ENST00000565038.2:c.*777_*778delinsCG	ENSP00000459882.2:n.*777_*778delinsCG
ENST00000566069.6:c.3202-4249_3202-4248delinsCG	ENSP00000459237.2:n.3202-4249_3202-4248delinsCG
ENST00000697377.2:c.3140_3141delinsCG	ENSP00000513286.2:p.Thr1047=
ENST00000697379.2:c.3302_3303delinsCG	ENSP00000513287.2:p.Thr1101=
ENST00000561514.2:c.2411_2412delinsCG	ENSP00000460666.2:p.Thr804=
ENST00000697374.1:c.2411_2412delinsCG	ENSP00000513284.1:p.Thr804=
ENST00000697375.1:n.4643_4644delinsCG
ENST00000697376.1:c.2317-4249_2317-4248delinsCG	ENSP00000513285.1:n.2317-4249_2317-4248delinsCG
ENST00000697377.1:c.2249_2250delinsCG	ENSP00000513286.1:p.Thr750=
ENST00000697378.1:n.3816_3817delinsCG
ENST00000697379.1:c.2411_2412delinsCG	ENSP00000513287.1:p.Thr804=
ENST00000697380.1:n.2500_2501delinsCG
ENST00000697381.1:n.1991_1992delinsCG
ENST00000697382.1:c.*73_*74delinsCG	ENSP00000513288.1:n.*73_*74delinsCG
ENST00000697383.1:c.830_831delinsCG	ENSP00000513289.1:p.Thr277=
ENST00000261584.9:c.3296_3297delinsCG MANE Select	ENSP00000261584.4:p.Thr1099=
ENST00000261584.8:c.3296_3297delinsCG	ENSP00000261584.4:p.Thr1099=
ENST00000566069.5:c.117-4249_117-4248delinsCG
ENST00000568219.5:c.2411_2412delinsCG	ENSP00000454703.2:p.Thr804=
NM_024675.3:c.3296_3297delinsCG , LRG_308t1:c.3296_3297delinsCG	NP_078951.2:p.Thr1099=
XM_011545946.1:c.3302_3303delinsCG	XP_011544248.1:p.Thr1101=
XM_011545947.1:c.3208-4249_3208-4248delinsCG	XP_011544249.1:n.3208-4249_3208-4248delinsCG
XM_011545948.1:c.2411_2412delinsCG	XP_011544250.1:p.Thr804=
XR_950851.1:n.4004_4005delinsCG
XM_011545946.2:c.3302_3303delinsCG	XP_011544248.1:p.Thr1101=
XM_011545947.2:c.3208-4249_3208-4248delinsCG	XP_011544249.1:n.3208-4249_3208-4248delinsCG
XM_011545948.2:c.2411_2412delinsCG	XP_011544250.1:p.Thr804=
XM_017023671.1:c.3120-4249_3120-4248delinsCG	XP_016879160.1:n.3120-4249_3120-4248delinsCG
XM_017023672.2:c.3114-4249_3114-4248delinsCG	XP_016879161.1:n.3114-4249_3114-4248delinsCG
XM_017023673.2:c.3202-4249_3202-4248delinsCG	XP_016879162.1:n.3202-4249_3202-4248delinsCG
NM_024675.4:c.3296_3297delinsCG MANE Select	NP_078951.2:p.Thr1099=