Canonical Allele Identifier: CA2213424418

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603565_23603568delinsGGGA , CM000678.2:g.23603565_23603568delinsGGGA	GRCh38
NC_000016.9:g.23614886_23614889delinsGGGA , CM000678.1:g.23614886_23614889delinsGGGA	GRCh37
NC_000016.8:g.23522387_23522390delinsGGGA	NCBI36
NG_007406.1:g.42790_42793delinsTCCC , LRG_308:g.42790_42793delinsTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3458_3461delinsTCCC	ENSP00000460666.3:p.Leu1153=
ENST00000565038.2:c.*937_*940delinsTCCC	ENSP00000459882.2:n.*937_*940delinsTCCC
ENST00000566069.6:c.*87_*90delinsTCCC	ENSP00000459237.2:n.*87_*90delinsTCCC
ENST00000697377.2:c.3296_3299delinsTCCC	ENSP00000513286.2:p.Leu1099=
ENST00000697379.2:c.3458_3461delinsTCCC	ENSP00000513287.2:p.Leu1153=
ENST00000561514.2:c.2567_2570delinsTCCC	ENSP00000460666.2:p.Leu856=
ENST00000697374.1:c.2567_2570delinsTCCC	ENSP00000513284.1:p.Leu856=
ENST00000697375.1:n.4799_4802delinsTCCC
ENST00000697376.1:c.*87_*90delinsTCCC	ENSP00000513285.1:n.*87_*90delinsTCCC
ENST00000697377.1:c.2405_2408delinsTCCC	ENSP00000513286.1:p.Leu802=
ENST00000697378.1:n.3972_3975delinsTCCC
ENST00000697379.1:c.2567_2570delinsTCCC	ENSP00000513287.1:p.Leu856=
ENST00000697380.1:n.2656_2659delinsTCCC
ENST00000697381.1:n.2147_2150delinsTCCC
ENST00000697382.1:c.*229_*232delinsTCCC	ENSP00000513288.1:n.*229_*232delinsTCCC
ENST00000697383.1:c.986_989delinsTCCC	ENSP00000513289.1:p.Leu329=
ENST00000261584.9:c.3452_3455delinsTCCC MANE Select	ENSP00000261584.4:p.Leu1151=
ENST00000261584.8:c.3452_3455delinsTCCC	ENSP00000261584.4:p.Leu1151=
ENST00000566069.5:c.218_221delinsTCCC
ENST00000568219.5:c.2567_2570delinsTCCC	ENSP00000454703.2:p.Leu856=
NM_024675.3:c.3452_3455delinsTCCC , LRG_308t1:c.3452_3455delinsTCCC	NP_078951.2:p.Leu1151=
XM_011545946.1:c.3458_3461delinsTCCC	XP_011544248.1:p.Leu1153=
XM_011545947.1:c.*87_*90delinsTCCC	XP_011544249.1:n.*87_*90delinsTCCC
XM_011545948.1:c.2567_2570delinsTCCC	XP_011544250.1:p.Leu856=
XR_950851.1:n.4160_4163delinsTCCC
XM_011545946.2:c.3458_3461delinsTCCC	XP_011544248.1:p.Leu1153=
XM_011545947.2:c.*87_*90delinsTCCC	XP_011544249.1:n.*87_*90delinsTCCC
XM_011545948.2:c.2567_2570delinsTCCC	XP_011544250.1:p.Leu856=
XM_017023671.1:c.3221_3224delinsTCCC	XP_016879160.1:p.Leu1074=
XM_017023672.2:c.3215_3218delinsTCCC	XP_016879161.1:p.Leu1072=
XM_017023673.2:c.*87_*90delinsTCCC	XP_016879162.1:n.*87_*90delinsTCCC
NM_024675.4:c.3452_3455delinsTCCC MANE Select	NP_078951.2:p.Leu1151=