Canonical Allele Identifier: CA2213409763
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621382_23621390delinsAATAGTAGT , CM000678.2:g.23621382_23621390delinsAATAGTAGT GRCh38
NC_000016.9:g.23632703_23632711delinsAATAGTAGT , CM000678.1:g.23632703_23632711delinsAATAGTAGT GRCh37
NC_000016.8:g.23540204_23540212delinsAATAGTAGT NCBI36
NG_007406.1:g.24968_24976delinsACTACTATT , LRG_308:g.24968_24976delinsACTACTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3091_3099delinsACTACTATT ENSP00000460666.3:p.Thr1031=
ENST00000565038.2:c.*566_*574delinsACTACTATT ENSP00000459882.2:n.*566_*574delinsACTACTATT
ENST00000566069.6:c.3085_3093delinsACTACTATT ENSP00000459237.2:p.Thr1029=
ENST00000697377.2:c.2929_2937delinsACTACTATT ENSP00000513286.2:p.Thr977=
ENST00000697379.2:c.3091_3099delinsACTACTATT ENSP00000513287.2:p.Thr1031=
ENST00000561514.2:c.2200_2208delinsACTACTATT ENSP00000460666.2:p.Thr734=
ENST00000697374.1:c.2200_2208delinsACTACTATT ENSP00000513284.1:p.Thr734=
ENST00000697375.1:n.4432_4440delinsACTACTATT
ENST00000697376.1:c.2200_2208delinsACTACTATT ENSP00000513285.1:p.Thr734=
ENST00000697377.1:c.2038_2046delinsACTACTATT ENSP00000513286.1:p.Thr680=
ENST00000697378.1:n.3605_3613delinsACTACTATT
ENST00000697379.1:c.2200_2208delinsACTACTATT ENSP00000513287.1:p.Thr734=
ENST00000697380.1:n.2377_2385delinsACTACTATT
ENST00000697381.1:n.1780_1788delinsACTACTATT
ENST00000697382.1:c.2200_2208delinsACTACTATT ENSP00000513288.1:p.Thr734=
ENST00000697383.1:c.619_627delinsACTACTATT ENSP00000513289.1:p.Thr207=
ENST00000261584.9:c.3085_3093delinsACTACTATT MANE Select ENSP00000261584.4:p.Thr1029=
ENST00000261584.8:c.3085_3093delinsACTACTATT ENSP00000261584.4:p.Thr1029=
ENST00000568219.5:c.2200_2208delinsACTACTATT ENSP00000454703.2:p.Thr734=
NM_024675.3:c.3085_3093delinsACTACTATT , LRG_308t1:c.3085_3093delinsACTACTATT NP_078951.2:p.Thr1029=
XM_011545946.1:c.3091_3099delinsACTACTATT XP_011544248.1:p.Thr1031=
XM_011545947.1:c.3091_3099delinsACTACTATT XP_011544249.1:p.Thr1031=
XM_011545948.1:c.2200_2208delinsACTACTATT XP_011544250.1:p.Thr734=
XR_950851.1:n.3881_3889delinsACTACTATT
XM_011545946.2:c.3091_3099delinsACTACTATT XP_011544248.1:p.Thr1031=
XM_011545947.2:c.3091_3099delinsACTACTATT XP_011544249.1:p.Thr1031=
XM_011545948.2:c.2200_2208delinsACTACTATT XP_011544250.1:p.Thr734=
XM_017023671.1:c.3091_3099delinsACTACTATT XP_016879160.1:p.Thr1031=
XM_017023672.2:c.3085_3093delinsACTACTATT XP_016879161.1:p.Thr1029=
XM_017023673.2:c.3085_3093delinsACTACTATT XP_016879162.1:p.Thr1029=
NM_024675.4:c.3085_3093delinsACTACTATT MANE Select NP_078951.2:p.Thr1029=