Canonical Allele Identifier: CA2213424587
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23630618C= , CM000678.2:g.23630618C= GRCh38
NC_000016.9:g.23641939C= , CM000678.1:g.23641939C= GRCh37
NC_000016.8:g.23549440C= NCBI36
NG_007406.1:g.15740G= , LRG_308:g.15740G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1691-149G= ENSP00000460666.3:n.1691-149G=
ENST00000565038.2:c.212-1343G= ENSP00000459882.2:n.212-1343G=
ENST00000566069.6:c.1685-149G= ENSP00000459237.2:n.1685-149G=
ENST00000697377.2:c.1691-149G= ENSP00000513286.2:n.1691-149G=
ENST00000697379.2:c.1691-149G= ENSP00000513287.2:n.1691-149G=
ENST00000561514.2:c.800-149G= ENSP00000460666.2:n.800-149G=
ENST00000697374.1:c.800-149G= ENSP00000513284.1:n.800-149G=
ENST00000697375.1:n.3032-149G=
ENST00000697376.1:c.800-149G= ENSP00000513285.1:n.800-149G=
ENST00000697377.1:c.800-149G= ENSP00000513286.1:n.800-149G=
ENST00000697378.1:n.2205-149G=
ENST00000697379.1:c.800-149G= ENSP00000513287.1:n.800-149G=
ENST00000697380.1:n.464G=
ENST00000697381.1:n.379+101G=
ENST00000697382.1:c.800-149G= ENSP00000513288.1:n.800-149G=
ENST00000697383.1:c.49-1343G= ENSP00000513289.1:n.49-1343G=
ENST00000697384.1:n.1839-149G=
ENST00000261584.9:c.1685-149G= MANE Select ENSP00000261584.4:n.1685-149G=
ENST00000261584.8:c.1685-149G= ENSP00000261584.4:n.1685-149G=
ENST00000565038.1:c.87-1343G=
ENST00000568219.5:c.800-149G= ENSP00000454703.2:n.800-149G=
NM_024675.3:c.1685-149G= , LRG_308t1:c.1685-149G= NP_078951.2:n.1685-149G=
XM_011545946.1:c.1691-149G= XP_011544248.1:n.1691-149G=
XM_011545947.1:c.1691-149G= XP_011544249.1:n.1691-149G=
XM_011545948.1:c.800-149G= XP_011544250.1:n.800-149G=
XR_950851.1:n.2481-149G=
XM_011545946.2:c.1691-149G= XP_011544248.1:n.1691-149G=
XM_011545947.2:c.1691-149G= XP_011544249.1:n.1691-149G=
XM_011545948.2:c.800-149G= XP_011544250.1:n.800-149G=
XM_017023671.1:c.1691-149G= XP_016879160.1:n.1691-149G=
XM_017023672.2:c.1685-149G= XP_016879161.1:n.1685-149G=
XM_017023673.2:c.1685-149G= XP_016879162.1:n.1685-149G=
NM_024675.4:c.1685-149G= MANE Select NP_078951.2:n.1685-149G=