Canonical Allele Identifier: CA2213412634

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623059_23623074delinsACAGCTTTTATATTTC , CM000678.2:g.23623059_23623074delinsACAGCTTTTATATTTC	GRCh38
NC_000016.9:g.23634380_23634395delinsACAGCTTTTATATTTC , CM000678.1:g.23634380_23634395delinsACAGCTTTTATATTTC	GRCh37
NC_000016.8:g.23541881_23541896delinsACAGCTTTTATATTTC	NCBI36
NG_007406.1:g.23284_23299delinsGAAATATAAAAGCTGT , LRG_308:g.23284_23299delinsGAAATATAAAAGCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2897_2912delinsGAAATATAAAAGCTGT	ENSP00000460666.3:p.Gly966=
ENST00000565038.2:c.*372_*387delinsGAAATATAAAAGCTGT	ENSP00000459882.2:n.*372_*387delinsGAAATATAAAAGCTGT
ENST00000566069.6:c.2891_2906delinsGAAATATAAAAGCTGT	ENSP00000459237.2:p.Gly964=
ENST00000697377.2:c.2735_2750delinsGAAATATAAAAGCTGT	ENSP00000513286.2:p.Gly912=
ENST00000697379.2:c.2897_2912delinsGAAATATAAAAGCTGT	ENSP00000513287.2:p.Gly966=
ENST00000561514.2:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000460666.2:p.Gly669=
ENST00000697374.1:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000513284.1:p.Gly669=
ENST00000697375.1:n.4238_4253delinsGAAATATAAAAGCTGT
ENST00000697376.1:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000513285.1:p.Gly669=
ENST00000697377.1:c.1844_1859delinsGAAATATAAAAGCTGT	ENSP00000513286.1:p.Gly615=
ENST00000697378.1:n.3411_3426delinsGAAATATAAAAGCTGT
ENST00000697379.1:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000513287.1:p.Gly669=
ENST00000697380.1:n.2183_2198delinsGAAATATAAAAGCTGT
ENST00000697381.1:n.1586_1601delinsGAAATATAAAAGCTGT
ENST00000697382.1:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000513288.1:p.Gly669=
ENST00000697383.1:c.425_440delinsGAAATATAAAAGCTGT	ENSP00000513289.1:p.Gly142=
ENST00000261584.9:c.2891_2906delinsGAAATATAAAAGCTGT MANE Select	ENSP00000261584.4:p.Gly964=
ENST00000261584.8:c.2891_2906delinsGAAATATAAAAGCTGT	ENSP00000261584.4:p.Gly964=
ENST00000568219.5:c.2006_2021delinsGAAATATAAAAGCTGT	ENSP00000454703.2:p.Gly669=
NM_024675.3:c.2891_2906delinsGAAATATAAAAGCTGT , LRG_308t1:c.2891_2906delinsGAAATATAAAAGCTGT	NP_078951.2:p.Gly964=
XM_011545946.1:c.2897_2912delinsGAAATATAAAAGCTGT	XP_011544248.1:p.Gly966=
XM_011545947.1:c.2897_2912delinsGAAATATAAAAGCTGT	XP_011544249.1:p.Gly966=
XM_011545948.1:c.2006_2021delinsGAAATATAAAAGCTGT	XP_011544250.1:p.Gly669=
XR_950851.1:n.3687_3702delinsGAAATATAAAAGCTGT
XM_011545946.2:c.2897_2912delinsGAAATATAAAAGCTGT	XP_011544248.1:p.Gly966=
XM_011545947.2:c.2897_2912delinsGAAATATAAAAGCTGT	XP_011544249.1:p.Gly966=
XM_011545948.2:c.2006_2021delinsGAAATATAAAAGCTGT	XP_011544250.1:p.Gly669=
XM_017023671.1:c.2897_2912delinsGAAATATAAAAGCTGT	XP_016879160.1:p.Gly966=
XM_017023672.2:c.2891_2906delinsGAAATATAAAAGCTGT	XP_016879161.1:p.Gly964=
XM_017023673.2:c.2891_2906delinsGAAATATAAAAGCTGT	XP_016879162.1:p.Gly964=
NM_024675.4:c.2891_2906delinsGAAATATAAAAGCTGT MANE Select	NP_078951.2:p.Gly964=