Canonical Allele Identifier: CA2632322970

Gene: PALB2

Linked Data

• gnomAD v4: 16-23607841-G-GAGTAGCAGTTATGCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607843_23607858dup , CM000678.2:g.23607843_23607858dup	GRCh38
NC_000016.9:g.23619164_23619179dup , CM000678.1:g.23619164_23619179dup	GRCh37
NC_000016.8:g.23526665_23526680dup	NCBI36
NG_007406.1:g.38501_38516dup , LRG_308:g.38501_38516dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3356+7_3356+22dup	ENSP00000460666.3:n.3356+7_3356+22dup
ENST00000565038.2:c.*835+3_*835+18dup	ENSP00000459882.2:n.*835+3_*835+18dup
ENST00000566069.6:c.3202-4188_3202-4173dup	ENSP00000459237.2:n.3202-4188_3202-4173du...
ENST00000697377.2:c.3194+7_3194+22dup	ENSP00000513286.2:n.3194+7_3194+22dup
ENST00000697379.2:c.3356+7_3356+22dup	ENSP00000513287.2:n.3356+7_3356+22dup
ENST00000561514.2:c.2465+7_2465+22dup	ENSP00000460666.2:n.2465+7_2465+22dup
ENST00000697374.1:c.2465+7_2465+22dup	ENSP00000513284.1:n.2465+7_2465+22dup
ENST00000697375.1:n.4697+7_4697+22dup
ENST00000697376.1:c.2317-4188_2317-4173dup	ENSP00000513285.1:n.2317-4188_2317-4173du...
ENST00000697377.1:c.2303+7_2303+22dup	ENSP00000513286.1:n.2303+7_2303+22dup
ENST00000697378.1:n.3870+7_3870+22dup
ENST00000697379.1:c.2465+7_2465+22dup	ENSP00000513287.1:n.2465+7_2465+22dup
ENST00000697380.1:n.2554+7_2554+22dup
ENST00000697381.1:n.2045+7_2045+22dup
ENST00000697382.1:c.*127+7_*127+22dup	ENSP00000513288.1:n.*127+7_*127+22dup
ENST00000697383.1:c.884+7_884+22dup	ENSP00000513289.1:n.884+7_884+22dup
ENST00000261584.9:c.3350+7_3350+22dup MANE Select	ENSP00000261584.4:n.3350+7_3350+22dup
ENST00000261584.8:c.3350+7_3350+22dup	ENSP00000261584.4:n.3350+7_3350+22dup
ENST00000566069.5:c.117-4188_117-4173dup
ENST00000568219.5:c.2465+7_2465+22dup	ENSP00000454703.2:n.2465+7_2465+22dup
NM_024675.3:c.3350+7_3350+22dup , LRG_308t1:c.3350+7_3350+22dup	NP_078951.2:n.3350+7_3350+22dup
XM_011545946.1:c.3356+7_3356+22dup	XP_011544248.1:n.3356+7_3356+22dup
XM_011545947.1:c.3208-4188_3208-4173dup	XP_011544249.1:n.3208-4188_3208-4173dup
XM_011545948.1:c.2465+7_2465+22dup	XP_011544250.1:n.2465+7_2465+22dup
XR_950851.1:n.4058+7_4058+22dup
XM_011545946.2:c.3356+7_3356+22dup	XP_011544248.1:n.3356+7_3356+22dup
XM_011545947.2:c.3208-4188_3208-4173dup	XP_011544249.1:n.3208-4188_3208-4173dup
XM_011545948.2:c.2465+7_2465+22dup	XP_011544250.1:n.2465+7_2465+22dup
XM_017023671.1:c.3120-4188_3120-4173dup	XP_016879160.1:n.3120-4188_3120-4173dup
XM_017023672.2:c.3114-4188_3114-4173dup	XP_016879161.1:n.3114-4188_3114-4173dup
XM_017023673.2:c.3202-4188_3202-4173dup	XP_016879162.1:n.3202-4188_3202-4173dup
NM_024675.4:c.3350+7_3350+22dup MANE Select	NP_078951.2:n.3350+7_3350+22dup