Canonical Allele Identifier: CA2632327913

Gene: PALB2

Linked Data

• gnomAD v4: 16-23634776-AAAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634784_23634787del , CM000678.2:g.23634784_23634787del	GRCh38
NC_000016.9:g.23646105_23646108del , CM000678.1:g.23646105_23646108del	GRCh37
NC_000016.8:g.23553606_23553609del	NCBI36
NG_007406.1:g.11578_11581del , LRG_308:g.11578_11581del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1690+82_1690+85del	ENSP00000460666.3:n.1690+82_1690+85del
ENST00000565038.2:c.211+3070_211+3073del	ENSP00000459882.2:n.211+3070_211+3073del
ENST00000566069.6:c.1684+82_1684+85del	ENSP00000459237.2:n.1684+82_1684+85del
ENST00000697377.2:c.1690+82_1690+85del	ENSP00000513286.2:n.1690+82_1690+85del
ENST00000697379.2:c.1690+82_1690+85del	ENSP00000513287.2:n.1690+82_1690+85del
ENST00000561514.2:c.799+82_799+85del	ENSP00000460666.2:n.799+82_799+85del
ENST00000697374.1:c.799+82_799+85del	ENSP00000513284.1:n.799+82_799+85del
ENST00000697375.1:n.3031+82_3031+85del
ENST00000697376.1:c.799+82_799+85del	ENSP00000513285.1:n.799+82_799+85del
ENST00000697377.1:c.799+82_799+85del	ENSP00000513286.1:n.799+82_799+85del
ENST00000697378.1:n.2204+82_2204+85del
ENST00000697379.1:c.799+82_799+85del	ENSP00000513287.1:n.799+82_799+85del
ENST00000697382.1:c.799+82_799+85del	ENSP00000513288.1:n.799+82_799+85del
ENST00000697383.1:c.49-5505_49-5502del	ENSP00000513289.1:n.49-5505_49-5502del
ENST00000697384.1:n.1838+82_1838+85del
ENST00000261584.9:c.1684+82_1684+85del MANE Select	ENSP00000261584.4:n.1684+82_1684+85del
ENST00000261584.8:c.1684+82_1684+85del	ENSP00000261584.4:n.1684+82_1684+85del
ENST00000565038.1:c.86+3070_86+3073del
ENST00000568219.5:c.799+82_799+85del	ENSP00000454703.2:n.799+82_799+85del
NM_024675.3:c.1684+82_1684+85del , LRG_308t1:c.1684+82_1684+85del	NP_078951.2:n.1684+82_1684+85del
XM_011545946.1:c.1690+82_1690+85del	XP_011544248.1:n.1690+82_1690+85del
XM_011545947.1:c.1690+82_1690+85del	XP_011544249.1:n.1690+82_1690+85del
XM_011545948.1:c.799+82_799+85del	XP_011544250.1:n.799+82_799+85del
XR_950851.1:n.2480+82_2480+85del
XM_011545946.2:c.1690+82_1690+85del	XP_011544248.1:n.1690+82_1690+85del
XM_011545947.2:c.1690+82_1690+85del	XP_011544249.1:n.1690+82_1690+85del
XM_011545948.2:c.799+82_799+85del	XP_011544250.1:n.799+82_799+85del
XM_017023671.1:c.1690+82_1690+85del	XP_016879160.1:n.1690+82_1690+85del
XM_017023672.2:c.1684+82_1684+85del	XP_016879161.1:n.1684+82_1684+85del
XM_017023673.2:c.1684+82_1684+85del	XP_016879162.1:n.1684+82_1684+85del
NM_024675.4:c.1684+82_1684+85del MANE Select	NP_078951.2:n.1684+82_1684+85del