Canonical Allele Identifier: CA2838032596

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607885_23607894delinsCAGG , CM000678.2:g.23607885_23607894delinsCAGG	GRCh38
NC_000016.9:g.23619206_23619215delinsCAGG , CM000678.1:g.23619206_23619215delinsCAGG	GRCh37
NC_000016.8:g.23526707_23526716delinsCAGG	NCBI36
NG_007406.1:g.38464_38473delinsCCTG , LRG_308:g.38464_38473delinsCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3326_3335delinsCCTG	ENSP00000460666.3:p.Leu1109_Leu1112delinsProCys
ENST00000565038.2:c.*801_*810delinsCCTG	ENSP00000459882.2:n.*801_*810delinsCCTG
ENST00000566069.6:c.3202-4225_3202-4216delinsCCTG	ENSP00000459237.2:n.3202-4225_3202-4216delinsCCTG
ENST00000697377.2:c.3164_3173delinsCCTG	ENSP00000513286.2:p.Leu1055_Leu1058delinsProCys
ENST00000697379.2:c.3326_3335delinsCCTG	ENSP00000513287.2:p.Leu1109_Leu1112delinsProCys
ENST00000561514.2:c.2435_2444delinsCCTG	ENSP00000460666.2:p.Leu812_Leu815delinsProCys
ENST00000697374.1:c.2435_2444delinsCCTG	ENSP00000513284.1:p.Leu812_Leu815delinsProCys
ENST00000697375.1:n.4667_4676delinsCCTG
ENST00000697376.1:c.2317-4225_2317-4216delinsCCTG	ENSP00000513285.1:n.2317-4225_2317-4216delinsCCTG
ENST00000697377.1:c.2273_2282delinsCCTG	ENSP00000513286.1:p.Leu758_Leu761delinsProCys
ENST00000697378.1:n.3840_3849delinsCCTG
ENST00000697379.1:c.2435_2444delinsCCTG	ENSP00000513287.1:p.Leu812_Leu815delinsProCys
ENST00000697380.1:n.2524_2533delinsCCTG
ENST00000697381.1:n.2015_2024delinsCCTG
ENST00000697382.1:c.*97_*106delinsCCTG	ENSP00000513288.1:n.*97_*106delinsCCTG
ENST00000697383.1:c.854_863delinsCCTG	ENSP00000513289.1:p.Leu285_Leu288delinsProCys
ENST00000261584.9:c.3320_3329delinsCCTG MANE Select	ENSP00000261584.4:p.Leu1107_Leu1110delinsProCys
ENST00000261584.8:c.3320_3329delinsCCTG	ENSP00000261584.4:p.Leu1107_Leu1110delinsProCys
ENST00000566069.5:c.117-4225_117-4216delinsCCTG
ENST00000568219.5:c.2435_2444delinsCCTG	ENSP00000454703.2:p.Leu812_Leu815delinsProCys
NM_024675.3:c.3320_3329delinsCCTG , LRG_308t1:c.3320_3329delinsCCTG	NP_078951.2:p.Leu1107_Leu1110delinsProCys
XM_011545946.1:c.3326_3335delinsCCTG	XP_011544248.1:p.Leu1109_Leu1112delinsProCys
XM_011545947.1:c.3208-4225_3208-4216delinsCCTG	XP_011544249.1:n.3208-4225_3208-4216delinsCCTG
XM_011545948.1:c.2435_2444delinsCCTG	XP_011544250.1:p.Leu812_Leu815delinsProCys
XR_950851.1:n.4028_4037delinsCCTG
XM_011545946.2:c.3326_3335delinsCCTG	XP_011544248.1:p.Leu1109_Leu1112delinsProCys
XM_011545947.2:c.3208-4225_3208-4216delinsCCTG	XP_011544249.1:n.3208-4225_3208-4216delinsCCTG
XM_011545948.2:c.2435_2444delinsCCTG	XP_011544250.1:p.Leu812_Leu815delinsProCys
XM_017023671.1:c.3120-4225_3120-4216delinsCCTG	XP_016879160.1:n.3120-4225_3120-4216delinsCCTG
XM_017023672.2:c.3114-4225_3114-4216delinsCCTG	XP_016879161.1:n.3114-4225_3114-4216delinsCCTG
XM_017023673.2:c.3202-4225_3202-4216delinsCCTG	XP_016879162.1:n.3202-4225_3202-4216delinsCCTG
NM_024675.4:c.3320_3329delinsCCTG MANE Select	NP_078951.2:p.Leu1107_Leu1110delinsProCys