Canonical Allele Identifier: CA2806270501

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624117_23624118insCACACCC , CM000678.2:g.23624117_23624118insCACACCC	GRCh38
NC_000016.9:g.23635438_23635439insCACACCC , CM000678.1:g.23635438_23635439insCACACCC	GRCh37
NC_000016.8:g.23542939_23542940insCACACCC	NCBI36
NG_007406.1:g.22240_22241insGGGTGTG , LRG_308:g.22240_22241insGGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2755-24_2755-23insGGGTGTG	ENSP00000460666.3:n.2755-24_2755-23insGGGTGTG
ENST00000565038.2:c.*230-24_*230-23insGGGTGTG	ENSP00000459882.2:n.*230-24_*230-23insGGGTGTG
ENST00000566069.6:c.2749-24_2749-23insGGGTGTG	ENSP00000459237.2:n.2749-24_2749-23insGGGTGTG
ENST00000697377.2:c.2593-24_2593-23insGGGTGTG	ENSP00000513286.2:n.2593-24_2593-23insGGGTGTG
ENST00000697379.2:c.2755-24_2755-23insGGGTGTG	ENSP00000513287.2:n.2755-24_2755-23insGGGTGTG
ENST00000561514.2:c.1864-24_1864-23insGGGTGTG	ENSP00000460666.2:n.1864-24_1864-23insGGGTGTG
ENST00000697374.1:c.1864-24_1864-23insGGGTGTG	ENSP00000513284.1:n.1864-24_1864-23insGGGTGTG
ENST00000697375.1:n.4096-24_4096-23insGGGTGTG
ENST00000697376.1:c.1864-24_1864-23insGGGTGTG	ENSP00000513285.1:n.1864-24_1864-23insGGGTGTG
ENST00000697377.1:c.1702-24_1702-23insGGGTGTG	ENSP00000513286.1:n.1702-24_1702-23insGGGTGTG
ENST00000697378.1:n.3269-24_3269-23insGGGTGTG
ENST00000697379.1:c.1864-24_1864-23insGGGTGTG	ENSP00000513287.1:n.1864-24_1864-23insGGGTGTG
ENST00000697380.1:n.2041-24_2041-23insGGGTGTG
ENST00000697381.1:n.1444-24_1444-23insGGGTGTG
ENST00000697382.1:c.1864-24_1864-23insGGGTGTG	ENSP00000513288.1:n.1864-24_1864-23insGGGTGTG
ENST00000697383.1:c.283-24_283-23insGGGTGTG	ENSP00000513289.1:n.283-24_283-23insGGGTGTG
ENST00000261584.9:c.2749-24_2749-23insGGGTGTG MANE Select	ENSP00000261584.4:n.2749-24_2749-23insGGGTGTG
ENST00000261584.8:c.2749-24_2749-23insGGGTGTG	ENSP00000261584.4:n.2749-24_2749-23insGGGTGTG
ENST00000565038.1:c.321-24_321-23insGGGTGTG
ENST00000568219.5:c.1864-24_1864-23insGGGTGTG	ENSP00000454703.2:n.1864-24_1864-23insGGGTGTG
NM_024675.3:c.2749-24_2749-23insGGGTGTG , LRG_308t1:c.2749-24_2749-23insGGGTGTG	NP_078951.2:n.2749-24_2749-23insGGGTGTG
XM_011545946.1:c.2755-24_2755-23insGGGTGTG	XP_011544248.1:n.2755-24_2755-23insGGGTGTG
XM_011545947.1:c.2755-24_2755-23insGGGTGTG	XP_011544249.1:n.2755-24_2755-23insGGGTGTG
XM_011545948.1:c.1864-24_1864-23insGGGTGTG	XP_011544250.1:n.1864-24_1864-23insGGGTGTG
XR_950851.1:n.3545-24_3545-23insGGGTGTG
XM_011545946.2:c.2755-24_2755-23insGGGTGTG	XP_011544248.1:n.2755-24_2755-23insGGGTGTG
XM_011545947.2:c.2755-24_2755-23insGGGTGTG	XP_011544249.1:n.2755-24_2755-23insGGGTGTG
XM_011545948.2:c.1864-24_1864-23insGGGTGTG	XP_011544250.1:n.1864-24_1864-23insGGGTGTG
XM_017023671.1:c.2755-24_2755-23insGGGTGTG	XP_016879160.1:n.2755-24_2755-23insGGGTGTG
XM_017023672.2:c.2749-24_2749-23insGGGTGTG	XP_016879161.1:n.2749-24_2749-23insGGGTGTG
XM_017023673.2:c.2749-24_2749-23insGGGTGTG	XP_016879162.1:n.2749-24_2749-23insGGGTGTG
NM_024675.4:c.2749-24_2749-23insGGGTGTG MANE Select	NP_078951.2:n.2749-24_2749-23insGGGTGTG