Canonical Allele Identifier: CA2213421864

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629683_23629684delinsCA , CM000678.2:g.23629683_23629684delinsCA	GRCh38
NC_000016.9:g.23641004_23641005delinsCA , CM000678.1:g.23641004_23641005delinsCA	GRCh37
NC_000016.8:g.23548505_23548506delinsCA	NCBI36
NG_007406.1:g.16674_16675delinsTG , LRG_308:g.16674_16675delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2476_2477delinsTG	ENSP00000460666.3:p.Cys826=
ENST00000565038.2:c.212-409_212-408delinsTG	ENSP00000459882.2:n.212-409_212-408delinsTG
ENST00000566069.6:c.2470_2471delinsTG	ENSP00000459237.2:p.Cys824=
ENST00000697377.2:c.2476_2477delinsTG	ENSP00000513286.2:p.Cys826=
ENST00000697379.2:c.2476_2477delinsTG	ENSP00000513287.2:p.Cys826=
ENST00000561514.2:c.1585_1586delinsTG	ENSP00000460666.2:p.Cys529=
ENST00000697374.1:c.1585_1586delinsTG	ENSP00000513284.1:p.Cys529=
ENST00000697375.1:n.3817_3818delinsTG
ENST00000697376.1:c.1585_1586delinsTG	ENSP00000513285.1:p.Cys529=
ENST00000697377.1:c.1585_1586delinsTG	ENSP00000513286.1:p.Cys529=
ENST00000697378.1:n.2990_2991delinsTG
ENST00000697379.1:c.1585_1586delinsTG	ENSP00000513287.1:p.Cys529=
ENST00000697380.1:n.1398_1399delinsTG
ENST00000697381.1:n.1165_1166delinsTG
ENST00000697382.1:c.1585_1586delinsTG	ENSP00000513288.1:p.Cys529=
ENST00000697383.1:c.49-409_49-408delinsTG	ENSP00000513289.1:n.49-409_49-408delinsTG
ENST00000697384.1:n.2624_2625delinsTG
ENST00000261584.9:c.2470_2471delinsTG MANE Select	ENSP00000261584.4:p.Cys824=
ENST00000261584.8:c.2470_2471delinsTG	ENSP00000261584.4:p.Cys824=
ENST00000565038.1:c.87-409_87-408delinsTG
ENST00000568219.5:c.1585_1586delinsTG	ENSP00000454703.2:p.Cys529=
NM_024675.3:c.2470_2471delinsTG , LRG_308t1:c.2470_2471delinsTG	NP_078951.2:p.Cys824=
XM_011545946.1:c.2476_2477delinsTG	XP_011544248.1:p.Cys826=
XM_011545947.1:c.2476_2477delinsTG	XP_011544249.1:p.Cys826=
XM_011545948.1:c.1585_1586delinsTG	XP_011544250.1:p.Cys529=
XR_950851.1:n.3266_3267delinsTG
XM_011545946.2:c.2476_2477delinsTG	XP_011544248.1:p.Cys826=
XM_011545947.2:c.2476_2477delinsTG	XP_011544249.1:p.Cys826=
XM_011545948.2:c.1585_1586delinsTG	XP_011544250.1:p.Cys529=
XM_017023671.1:c.2476_2477delinsTG	XP_016879160.1:p.Cys826=
XM_017023672.2:c.2470_2471delinsTG	XP_016879161.1:p.Cys824=
XM_017023673.2:c.2470_2471delinsTG	XP_016879162.1:p.Cys824=
NM_024675.4:c.2470_2471delinsTG MANE Select	NP_078951.2:p.Cys824=