Canonical Allele Identifier: CA2213432488

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636316_23636318delinsCAT , CM000678.2:g.23636316_23636318delinsCAT	GRCh38
NC_000016.9:g.23647637_23647639delinsCAT , CM000678.1:g.23647637_23647639delinsCAT	GRCh37
NC_000016.8:g.23555138_23555140delinsCAT	NCBI36
NG_007406.1:g.10040_10042delinsATG , LRG_308:g.10040_10042delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.234_236delinsATG	ENSP00000460666.3:p.Ile78=
ENST00000565038.2:c.211+1532_211+1534delinsATG	ENSP00000459882.2:n.211+1532_211+1534delinsATG
ENST00000566069.6:c.228_230delinsATG	ENSP00000459237.2:p.Ile76=
ENST00000697377.2:c.234_236delinsATG	ENSP00000513286.2:p.Ile78=
ENST00000697379.2:c.234_236delinsATG	ENSP00000513287.2:p.Ile78=
ENST00000561514.2:c.-658_-656delinsATG	ENSP00000460666.2:n.-658_-656delinsATG
ENST00000697374.1:c.-658_-656delinsATG	ENSP00000513284.1:n.-658_-656delinsATG
ENST00000697375.1:n.1575_1577delinsATG
ENST00000697376.1:c.-658_-656delinsATG	ENSP00000513285.1:n.-658_-656delinsATG
ENST00000697377.1:c.-658_-656delinsATG	ENSP00000513286.1:n.-658_-656delinsATG
ENST00000697378.1:n.748_750delinsATG
ENST00000697379.1:c.-658_-656delinsATG	ENSP00000513287.1:n.-658_-656delinsATG
ENST00000697382.1:c.-658_-656delinsATG	ENSP00000513288.1:n.-658_-656delinsATG
ENST00000697383.1:c.48+4792_48+4794delinsATG	ENSP00000513289.1:n.48+4792_48+4794delinsATG
ENST00000697384.1:n.382_384delinsATG
ENST00000261584.9:c.228_230delinsATG MANE Select	ENSP00000261584.4:p.Ile76=
ENST00000261584.8:c.228_230delinsATG	ENSP00000261584.4:p.Ile76=
ENST00000561514.1:c.234_236delinsATG	ENSP00000460666.1:p.Ile78=
ENST00000565038.1:c.86+1532_86+1534delinsATG
ENST00000567003.1:n.506_508delinsATG
ENST00000568219.5:c.-658_-656delinsATG	ENSP00000454703.2:n.-658_-656delinsATG
NM_024675.3:c.228_230delinsATG , LRG_308t1:c.228_230delinsATG	NP_078951.2:p.Ile76=
XM_011545946.1:c.234_236delinsATG	XP_011544248.1:p.Ile78=
XM_011545947.1:c.234_236delinsATG	XP_011544249.1:p.Ile78=
XM_011545948.1:c.-658_-656delinsATG	XP_011544250.1:n.-658_-656delinsATG
XR_950851.1:n.1024_1026delinsATG
XM_011545946.2:c.234_236delinsATG	XP_011544248.1:p.Ile78=
XM_011545947.2:c.234_236delinsATG	XP_011544249.1:p.Ile78=
XM_011545948.2:c.-658_-656delinsATG	XP_011544250.1:n.-658_-656delinsATG
XM_017023671.1:c.234_236delinsATG	XP_016879160.1:p.Ile78=
XM_017023672.2:c.228_230delinsATG	XP_016879161.1:p.Ile76=
XM_017023673.2:c.228_230delinsATG	XP_016879162.1:p.Ile76=
NM_024675.4:c.228_230delinsATG MANE Select	NP_078951.2:p.Ile76=