Canonical Allele Identifier: CA2632327894

Gene: PALB2

Linked Data

• gnomAD v4: 16-23634761-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634762_23634763del , CM000678.2:g.23634762_23634763del	GRCh38
NC_000016.9:g.23646083_23646084del , CM000678.1:g.23646083_23646084del	GRCh37
NC_000016.8:g.23553584_23553585del	NCBI36
NG_007406.1:g.11595_11596del , LRG_308:g.11595_11596del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1690+99_1690+100del	ENSP00000460666.3:n.1690+99_1690+100del
ENST00000565038.2:c.211+3087_211+3088del	ENSP00000459882.2:n.211+3087_211+3088del
ENST00000566069.6:c.1684+99_1684+100del	ENSP00000459237.2:n.1684+99_1684+100del
ENST00000697377.2:c.1690+99_1690+100del	ENSP00000513286.2:n.1690+99_1690+100del
ENST00000697379.2:c.1690+99_1690+100del	ENSP00000513287.2:n.1690+99_1690+100del
ENST00000561514.2:c.799+99_799+100del	ENSP00000460666.2:n.799+99_799+100del
ENST00000697374.1:c.799+99_799+100del	ENSP00000513284.1:n.799+99_799+100del
ENST00000697375.1:n.3031+99_3031+100del
ENST00000697376.1:c.799+99_799+100del	ENSP00000513285.1:n.799+99_799+100del
ENST00000697377.1:c.799+99_799+100del	ENSP00000513286.1:n.799+99_799+100del
ENST00000697378.1:n.2204+99_2204+100del
ENST00000697379.1:c.799+99_799+100del	ENSP00000513287.1:n.799+99_799+100del
ENST00000697382.1:c.799+99_799+100del	ENSP00000513288.1:n.799+99_799+100del
ENST00000697383.1:c.49-5488_49-5487del	ENSP00000513289.1:n.49-5488_49-5487del
ENST00000697384.1:n.1838+99_1838+100del
ENST00000261584.9:c.1684+99_1684+100del MANE Select	ENSP00000261584.4:n.1684+99_1684+100del
ENST00000261584.8:c.1684+99_1684+100del	ENSP00000261584.4:n.1684+99_1684+100del
ENST00000565038.1:c.86+3087_86+3088del
ENST00000568219.5:c.799+99_799+100del	ENSP00000454703.2:n.799+99_799+100del
NM_024675.3:c.1684+99_1684+100del , LRG_308t1:c.1684+99_1684+100del	NP_078951.2:n.1684+99_1684+100del
XM_011545946.1:c.1690+99_1690+100del	XP_011544248.1:n.1690+99_1690+100del
XM_011545947.1:c.1690+99_1690+100del	XP_011544249.1:n.1690+99_1690+100del
XM_011545948.1:c.799+99_799+100del	XP_011544250.1:n.799+99_799+100del
XR_950851.1:n.2480+99_2480+100del
XM_011545946.2:c.1690+99_1690+100del	XP_011544248.1:n.1690+99_1690+100del
XM_011545947.2:c.1690+99_1690+100del	XP_011544249.1:n.1690+99_1690+100del
XM_011545948.2:c.799+99_799+100del	XP_011544250.1:n.799+99_799+100del
XM_017023671.1:c.1690+99_1690+100del	XP_016879160.1:n.1690+99_1690+100del
XM_017023672.2:c.1684+99_1684+100del	XP_016879161.1:n.1684+99_1684+100del
XM_017023673.2:c.1684+99_1684+100del	XP_016879162.1:n.1684+99_1684+100del
NM_024675.4:c.1684+99_1684+100del MANE Select	NP_078951.2:n.1684+99_1684+100del