Canonical Allele Identifier: CA2695222900

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607916_23607917insTAGGGTT , CM000678.2:g.23607916_23607917insTAGGGTT	GRCh38
NC_000016.9:g.23619237_23619238insTAGGGTT , CM000678.1:g.23619237_23619238insTAGGGTT	GRCh37
NC_000016.8:g.23526738_23526739insTAGGGTT	NCBI36
NG_007406.1:g.38442_38443insACCCTAA , LRG_308:g.38442_38443insACCCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3304_3305insACCCTAA	ENSP00000460666.3:p.Thr1102AsnfsTer25
ENST00000565038.2:c.*779_*780insACCCTAA	ENSP00000459882.2:n.*779_*780insACCCTAA
ENST00000566069.6:c.3202-4247_3202-4246insACCCTAA	ENSP00000459237.2:n.3202-4247_3202-4246insACCCTAA
ENST00000697377.2:c.3142_3143insACCCTAA	ENSP00000513286.2:p.Thr1048AsnfsTer25
ENST00000697379.2:c.3304_3305insACCCTAA	ENSP00000513287.2:p.Thr1102AsnfsTer25
ENST00000561514.2:c.2413_2414insACCCTAA	ENSP00000460666.2:p.Thr805AsnfsTer25
ENST00000697374.1:c.2413_2414insACCCTAA	ENSP00000513284.1:p.Thr805AsnfsTer25
ENST00000697375.1:n.4645_4646insACCCTAA
ENST00000697376.1:c.2317-4247_2317-4246insACCCTAA	ENSP00000513285.1:n.2317-4247_2317-4246insACCCTAA
ENST00000697377.1:c.2251_2252insACCCTAA	ENSP00000513286.1:p.Thr751AsnfsTer25
ENST00000697378.1:n.3818_3819insACCCTAA
ENST00000697379.1:c.2413_2414insACCCTAA	ENSP00000513287.1:p.Thr805AsnfsTer25
ENST00000697380.1:n.2502_2503insACCCTAA
ENST00000697381.1:n.1993_1994insACCCTAA
ENST00000697382.1:c.*75_*76insACCCTAA	ENSP00000513288.1:n.*75_*76insACCCTAA
ENST00000697383.1:c.832_833insACCCTAA	ENSP00000513289.1:p.Thr278AsnfsTer25
ENST00000261584.9:c.3298_3299insACCCTAA MANE Select	ENSP00000261584.4:p.Thr1100AsnfsTer25
ENST00000261584.8:c.3298_3299insACCCTAA	ENSP00000261584.4:p.Thr1100AsnfsTer25
ENST00000566069.5:c.117-4247_117-4246insACCCTAA
ENST00000568219.5:c.2413_2414insACCCTAA	ENSP00000454703.2:p.Thr805AsnfsTer25
NM_024675.3:c.3298_3299insACCCTAA , LRG_308t1:c.3298_3299insACCCTAA	NP_078951.2:p.Thr1100AsnfsTer25
XM_011545946.1:c.3304_3305insACCCTAA	XP_011544248.1:p.Thr1102AsnfsTer25
XM_011545947.1:c.3208-4247_3208-4246insACCCTAA	XP_011544249.1:n.3208-4247_3208-4246insACCCTAA
XM_011545948.1:c.2413_2414insACCCTAA	XP_011544250.1:p.Thr805AsnfsTer25
XR_950851.1:n.4006_4007insACCCTAA
XM_011545946.2:c.3304_3305insACCCTAA	XP_011544248.1:p.Thr1102AsnfsTer25
XM_011545947.2:c.3208-4247_3208-4246insACCCTAA	XP_011544249.1:n.3208-4247_3208-4246insACCCTAA
XM_011545948.2:c.2413_2414insACCCTAA	XP_011544250.1:p.Thr805AsnfsTer25
XM_017023671.1:c.3120-4247_3120-4246insACCCTAA	XP_016879160.1:n.3120-4247_3120-4246insACCCTAA
XM_017023672.2:c.3114-4247_3114-4246insACCCTAA	XP_016879161.1:n.3114-4247_3114-4246insACCCTAA
XM_017023673.2:c.3202-4247_3202-4246insACCCTAA	XP_016879162.1:n.3202-4247_3202-4246insACCCTAA
NM_024675.4:c.3298_3299insACCCTAA MANE Select	NP_078951.2:p.Thr1100AsnfsTer25