Canonical Allele Identifier: CA2632327917

Gene: PALB2

Linked Data

• gnomAD v4: 16-23634779-AGAAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634780_23634784del , CM000678.2:g.23634780_23634784del	GRCh38
NC_000016.9:g.23646101_23646105del , CM000678.1:g.23646101_23646105del	GRCh37
NC_000016.8:g.23553602_23553606del	NCBI36
NG_007406.1:g.11574_11578del , LRG_308:g.11574_11578del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1690+78_1690+82del	ENSP00000460666.3:n.1690+78_1690+82del
ENST00000565038.2:c.211+3066_211+3070del	ENSP00000459882.2:n.211+3066_211+3070del
ENST00000566069.6:c.1684+78_1684+82del	ENSP00000459237.2:n.1684+78_1684+82del
ENST00000697377.2:c.1690+78_1690+82del	ENSP00000513286.2:n.1690+78_1690+82del
ENST00000697379.2:c.1690+78_1690+82del	ENSP00000513287.2:n.1690+78_1690+82del
ENST00000561514.2:c.799+78_799+82del	ENSP00000460666.2:n.799+78_799+82del
ENST00000697374.1:c.799+78_799+82del	ENSP00000513284.1:n.799+78_799+82del
ENST00000697375.1:n.3031+78_3031+82del
ENST00000697376.1:c.799+78_799+82del	ENSP00000513285.1:n.799+78_799+82del
ENST00000697377.1:c.799+78_799+82del	ENSP00000513286.1:n.799+78_799+82del
ENST00000697378.1:n.2204+78_2204+82del
ENST00000697379.1:c.799+78_799+82del	ENSP00000513287.1:n.799+78_799+82del
ENST00000697382.1:c.799+78_799+82del	ENSP00000513288.1:n.799+78_799+82del
ENST00000697383.1:c.49-5509_49-5505del	ENSP00000513289.1:n.49-5509_49-5505del
ENST00000697384.1:n.1838+78_1838+82del
ENST00000261584.9:c.1684+78_1684+82del MANE Select	ENSP00000261584.4:n.1684+78_1684+82del
ENST00000261584.8:c.1684+78_1684+82del	ENSP00000261584.4:n.1684+78_1684+82del
ENST00000565038.1:c.86+3066_86+3070del
ENST00000568219.5:c.799+78_799+82del	ENSP00000454703.2:n.799+78_799+82del
NM_024675.3:c.1684+78_1684+82del , LRG_308t1:c.1684+78_1684+82del	NP_078951.2:n.1684+78_1684+82del
XM_011545946.1:c.1690+78_1690+82del	XP_011544248.1:n.1690+78_1690+82del
XM_011545947.1:c.1690+78_1690+82del	XP_011544249.1:n.1690+78_1690+82del
XM_011545948.1:c.799+78_799+82del	XP_011544250.1:n.799+78_799+82del
XR_950851.1:n.2480+78_2480+82del
XM_011545946.2:c.1690+78_1690+82del	XP_011544248.1:n.1690+78_1690+82del
XM_011545947.2:c.1690+78_1690+82del	XP_011544249.1:n.1690+78_1690+82del
XM_011545948.2:c.799+78_799+82del	XP_011544250.1:n.799+78_799+82del
XM_017023671.1:c.1690+78_1690+82del	XP_016879160.1:n.1690+78_1690+82del
XM_017023672.2:c.1684+78_1684+82del	XP_016879161.1:n.1684+78_1684+82del
XM_017023673.2:c.1684+78_1684+82del	XP_016879162.1:n.1684+78_1684+82del
NM_024675.4:c.1684+78_1684+82del MANE Select	NP_078951.2:n.1684+78_1684+82del