Canonical Allele Identifier: CA2213433813
Community Standard Title: NM_024675.4(PALB2):c.172T= (p.Leu58=)
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23637889A= , CM000678.2:g.23637889A= GRCh38
NC_000016.9:g.23649210A= , CM000678.1:g.23649210A= GRCh37
NC_000016.8:g.23556711A= NCBI36
NG_007406.1:g.8469T= , LRG_308:g.8469T=

Transcript Alleles

HGVS Amino-acid Change
NM_024675.4:c.172T= MANE Select NP_078951.2:p.Leu58=
ENST00000261584.9:c.172T= MANE Select ENSP00000261584.4:p.Leu58=
NM_024675.3:c.172T= , LRG_308t1:c.172T= NP_078951.2:p.Leu58=
ENST00000261584.8:c.172T= ENSP00000261584.4:p.Leu58=
ENST00000561514.1:c.178T= ENSP00000460666.1:p.Leu60=
ENST00000561514.2:c.-714T= ENSP00000460666.2:n.-714T=
ENST00000561514.3:c.178T= ENSP00000460666.3:p.Leu60=
ENST00000565038.1:c.47T=
ENST00000565038.2:c.172T= ENSP00000459882.2:p.Leu58=
ENST00000566069.6:c.172T= ENSP00000459237.2:p.Leu58=
ENST00000567003.1:n.450T=
ENST00000568219.5:c.-714T= ENSP00000454703.2:n.-714T=
ENST00000697374.1:c.-714T= ENSP00000513284.1:n.-714T=
ENST00000697375.1:n.1519T=
ENST00000697376.1:c.-714T= ENSP00000513285.1:n.-714T=
ENST00000697377.1:c.-714T= ENSP00000513286.1:n.-714T=
ENST00000697377.2:c.178T= ENSP00000513286.2:p.Leu60=
ENST00000697378.1:n.692T=
ENST00000697379.1:c.-714T= ENSP00000513287.1:n.-714T=
ENST00000697379.2:c.178T= ENSP00000513287.2:p.Leu60=
ENST00000697382.1:c.-714T= ENSP00000513288.1:n.-714T=
ENST00000697383.1:c.48+3221T= ENSP00000513289.1:n.48+3221T=
ENST00000697384.1:n.326T=
XM_011545946.1:c.178T= XP_011544248.1:p.Leu60=
XM_011545946.2:c.178T= XP_011544248.1:p.Leu60=
XM_011545947.1:c.178T= XP_011544249.1:p.Leu60=
XM_011545947.2:c.178T= XP_011544249.1:p.Leu60=
XM_011545948.1:c.-714T= XP_011544250.1:n.-714T=
XM_011545948.2:c.-714T= XP_011544250.1:n.-714T=
XM_017023671.1:c.178T= XP_016879160.1:p.Leu60=
XM_017023672.2:c.172T= XP_016879161.1:p.Leu58=
XM_017023673.2:c.172T= XP_016879162.1:p.Leu58=
XR_950851.1:n.968T=