Canonical Allele Identifier: CA2213434194

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23638016_23638017delinsGT , CM000678.2:g.23638016_23638017delinsGT	GRCh38
NC_000016.9:g.23649337_23649338delinsGT , CM000678.1:g.23649337_23649338delinsGT	GRCh37
NC_000016.8:g.23556838_23556839delinsGT	NCBI36
NG_007406.1:g.8341_8342delinsAC , LRG_308:g.8341_8342delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.114+53_114+54delinsAC	ENSP00000460666.3:n.114+53_114+54delinsAC
ENST00000565038.2:c.108+53_108+54delinsAC	ENSP00000459882.2:n.108+53_108+54delinsAC
ENST00000566069.6:c.108+53_108+54delinsAC	ENSP00000459237.2:n.108+53_108+54delinsAC
ENST00000697377.2:c.114+53_114+54delinsAC	ENSP00000513286.2:n.114+53_114+54delinsAC
ENST00000697379.2:c.114+53_114+54delinsAC	ENSP00000513287.2:n.114+53_114+54delinsAC
ENST00000561514.2:c.-778+53_-778+54delinsAC	ENSP00000460666.2:n.-778+53_-778+54delinsAC
ENST00000697374.1:c.-778+53_-778+54delinsAC	ENSP00000513284.1:n.-778+53_-778+54delinsAC
ENST00000697375.1:n.1455+53_1455+54delinsAC
ENST00000697376.1:c.-813-29_-813-28delinsAC	ENSP00000513285.1:n.-813-29_-813-28delinsAC
ENST00000697377.1:c.-778+53_-778+54delinsAC	ENSP00000513286.1:n.-778+53_-778+54delinsAC
ENST00000697378.1:n.628+53_628+54delinsAC
ENST00000697379.1:c.-778+53_-778+54delinsAC	ENSP00000513287.1:n.-778+53_-778+54delinsAC
ENST00000697382.1:c.-778+53_-778+54delinsAC	ENSP00000513288.1:n.-778+53_-778+54delinsAC
ENST00000697383.1:c.48+3093_48+3094delinsAC	ENSP00000513289.1:n.48+3093_48+3094delinsAC
ENST00000697384.1:n.262+53_262+54delinsAC
ENST00000261584.9:c.108+53_108+54delinsAC MANE Select	ENSP00000261584.4:n.108+53_108+54delinsAC
ENST00000261584.8:c.108+53_108+54delinsAC	ENSP00000261584.4:n.108+53_108+54delinsAC
ENST00000561514.1:c.114+53_114+54delinsAC	ENSP00000460666.1:n.114+53_114+54delinsAC
ENST00000567003.1:n.386+53_386+54delinsAC
ENST00000568219.5:c.-778+53_-778+54delinsAC	ENSP00000454703.2:n.-778+53_-778+54delinsAC
NM_024675.3:c.108+53_108+54delinsAC , LRG_308t1:c.108+53_108+54delinsAC	NP_078951.2:n.108+53_108+54delinsAC
XM_011545946.1:c.114+53_114+54delinsAC	XP_011544248.1:n.114+53_114+54delinsAC
XM_011545947.1:c.114+53_114+54delinsAC	XP_011544249.1:n.114+53_114+54delinsAC
XM_011545948.1:c.-778+53_-778+54delinsAC	XP_011544250.1:n.-778+53_-778+54delinsAC
XR_950851.1:n.904+53_904+54delinsAC
XM_011545946.2:c.114+53_114+54delinsAC	XP_011544248.1:n.114+53_114+54delinsAC
XM_011545947.2:c.114+53_114+54delinsAC	XP_011544249.1:n.114+53_114+54delinsAC
XM_011545948.2:c.-778+53_-778+54delinsAC	XP_011544250.1:n.-778+53_-778+54delinsAC
XM_017023671.1:c.114+53_114+54delinsAC	XP_016879160.1:n.114+53_114+54delinsAC
XM_017023672.2:c.108+53_108+54delinsAC	XP_016879161.1:n.108+53_108+54delinsAC
XM_017023673.2:c.108+53_108+54delinsAC	XP_016879162.1:n.108+53_108+54delinsAC
NM_024675.4:c.108+53_108+54delinsAC MANE Select	NP_078951.2:n.108+53_108+54delinsAC