Canonical Allele Identifier: CA2632327705

Gene: PALB2

Linked Data

• gnomAD v4: 16-23624063-T-TCAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624066_23624069dup , CM000678.2:g.23624066_23624069dup	GRCh38
NC_000016.9:g.23635387_23635390dup , CM000678.1:g.23635387_23635390dup	GRCh37
NC_000016.8:g.23542888_23542891dup	NCBI36
NG_007406.1:g.22291_22294dup , LRG_308:g.22291_22294dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2782_2785dup	ENSP00000460666.3:p.Asp929AlafsTer2
ENST00000565038.2:c.*257_*260dup	ENSP00000459882.2:n.*257_*260dup
ENST00000566069.6:c.2776_2779dup	ENSP00000459237.2:p.Asp927AlafsTer2
ENST00000697377.2:c.2620_2623dup	ENSP00000513286.2:p.Asp875AlafsTer2
ENST00000697379.2:c.2782_2785dup	ENSP00000513287.2:p.Asp929AlafsTer2
ENST00000561514.2:c.1891_1894dup	ENSP00000460666.2:p.Asp632AlafsTer2
ENST00000697374.1:c.1891_1894dup	ENSP00000513284.1:p.Asp632AlafsTer2
ENST00000697375.1:n.4123_4126dup
ENST00000697376.1:c.1891_1894dup	ENSP00000513285.1:p.Asp632AlafsTer2
ENST00000697377.1:c.1729_1732dup	ENSP00000513286.1:p.Asp578AlafsTer2
ENST00000697378.1:n.3296_3299dup
ENST00000697379.1:c.1891_1894dup	ENSP00000513287.1:p.Asp632AlafsTer2
ENST00000697380.1:n.2068_2071dup
ENST00000697381.1:n.1471_1474dup
ENST00000697382.1:c.1891_1894dup	ENSP00000513288.1:p.Asp632AlafsTer2
ENST00000697383.1:c.310_313dup	ENSP00000513289.1:p.Asp105AlafsTer2
ENST00000261584.9:c.2776_2779dup MANE Select	ENSP00000261584.4:p.Asp927AlafsTer2
ENST00000261584.8:c.2776_2779dup	ENSP00000261584.4:p.Asp927AlafsTer2
ENST00000568219.5:c.1891_1894dup	ENSP00000454703.2:p.Asp632AlafsTer2
NM_024675.3:c.2776_2779dup , LRG_308t1:c.2776_2779dup	NP_078951.2:p.Asp927AlafsTer2
XM_011545946.1:c.2782_2785dup	XP_011544248.1:p.Asp929AlafsTer2
XM_011545947.1:c.2782_2785dup	XP_011544249.1:p.Asp929AlafsTer2
XM_011545948.1:c.1891_1894dup	XP_011544250.1:p.Asp632AlafsTer2
XR_950851.1:n.3572_3575dup
XM_011545946.2:c.2782_2785dup	XP_011544248.1:p.Asp929AlafsTer2
XM_011545947.2:c.2782_2785dup	XP_011544249.1:p.Asp929AlafsTer2
XM_011545948.2:c.1891_1894dup	XP_011544250.1:p.Asp632AlafsTer2
XM_017023671.1:c.2782_2785dup	XP_016879160.1:p.Asp929AlafsTer2
XM_017023672.2:c.2776_2779dup	XP_016879161.1:p.Asp927AlafsTer2
XM_017023673.2:c.2776_2779dup	XP_016879162.1:p.Asp927AlafsTer2
NM_024675.4:c.2776_2779dup MANE Select	NP_078951.2:p.Asp927AlafsTer2