Canonical Allele Identifier: CA2632322992

Gene: PALB2

Linked Data

• gnomAD v4: 16-23607857-C-CACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607858_23607861dup , CM000678.2:g.23607858_23607861dup	GRCh38
NC_000016.9:g.23619179_23619182dup , CM000678.1:g.23619179_23619182dup	GRCh37
NC_000016.8:g.23526680_23526683dup	NCBI36
NG_007406.1:g.38497_38500dup , LRG_308:g.38497_38500dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3356+3_3356+6dup	ENSP00000460666.3:n.3356+3_3356+6dup
ENST00000565038.2:c.*834_*835+2dup
ENST00000566069.6:c.3202-4192_3202-4189dup	ENSP00000459237.2:n.3202-4192_3202-4189du...
ENST00000697377.2:c.3194+3_3194+6dup	ENSP00000513286.2:n.3194+3_3194+6dup
ENST00000697379.2:c.3356+3_3356+6dup	ENSP00000513287.2:n.3356+3_3356+6dup
ENST00000561514.2:c.2465+3_2465+6dup	ENSP00000460666.2:n.2465+3_2465+6dup
ENST00000697374.1:c.2465+3_2465+6dup	ENSP00000513284.1:n.2465+3_2465+6dup
ENST00000697375.1:n.4697+3_4697+6dup
ENST00000697376.1:c.2317-4192_2317-4189dup	ENSP00000513285.1:n.2317-4192_2317-4189du...
ENST00000697377.1:c.2303+3_2303+6dup	ENSP00000513286.1:n.2303+3_2303+6dup
ENST00000697378.1:n.3870+3_3870+6dup
ENST00000697379.1:c.2465+3_2465+6dup	ENSP00000513287.1:n.2465+3_2465+6dup
ENST00000697380.1:n.2554+3_2554+6dup
ENST00000697381.1:n.2045+3_2045+6dup
ENST00000697382.1:c.*127+3_*127+6dup	ENSP00000513288.1:n.*127+3_*127+6dup
ENST00000697383.1:c.884+3_884+6dup	ENSP00000513289.1:n.884+3_884+6dup
ENST00000261584.9:c.3350+3_3350+6dup MANE Select	ENSP00000261584.4:n.3350+3_3350+6dup
ENST00000261584.8:c.3350+3_3350+6dup	ENSP00000261584.4:n.3350+3_3350+6dup
ENST00000566069.5:c.117-4192_117-4189dup
ENST00000568219.5:c.2465+3_2465+6dup	ENSP00000454703.2:n.2465+3_2465+6dup
NM_024675.3:c.3350+3_3350+6dup , LRG_308t1:c.3350+3_3350+6dup	NP_078951.2:n.3350+3_3350+6dup
XM_011545946.1:c.3356+3_3356+6dup	XP_011544248.1:n.3356+3_3356+6dup
XM_011545947.1:c.3208-4192_3208-4189dup	XP_011544249.1:n.3208-4192_3208-4189dup
XM_011545948.1:c.2465+3_2465+6dup	XP_011544250.1:n.2465+3_2465+6dup
XR_950851.1:n.4058+3_4058+6dup
XM_011545946.2:c.3356+3_3356+6dup	XP_011544248.1:n.3356+3_3356+6dup
XM_011545947.2:c.3208-4192_3208-4189dup	XP_011544249.1:n.3208-4192_3208-4189dup
XM_011545948.2:c.2465+3_2465+6dup	XP_011544250.1:n.2465+3_2465+6dup
XM_017023671.1:c.3120-4192_3120-4189dup	XP_016879160.1:n.3120-4192_3120-4189dup
XM_017023672.2:c.3114-4192_3114-4189dup	XP_016879161.1:n.3114-4192_3114-4189dup
XM_017023673.2:c.3202-4192_3202-4189dup	XP_016879162.1:n.3202-4192_3202-4189dup
NM_024675.4:c.3350+3_3350+6dup MANE Select	NP_078951.2:n.3350+3_3350+6dup