Canonical Allele Identifier: CA2695222895

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603468_23603471delinsCAAA , CM000678.2:g.23603468_23603471delinsCAAA	GRCh38
NC_000016.9:g.23614789_23614792delinsCAAA , CM000678.1:g.23614789_23614792delinsCAAA	GRCh37
NC_000016.8:g.23522290_23522293delinsCAAA	NCBI36
NG_007406.1:g.42887_42890delinsTTTG , LRG_308:g.42887_42890delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3555_3558delinsTTTG	ENSP00000460666.3:p.His1186Leu
ENST00000565038.2:c.*1034_*1037delinsTTTG	ENSP00000459882.2:n.*1034_*1037delinsTTTG
ENST00000566069.6:c.*184_*187delinsTTTG	ENSP00000459237.2:n.*184_*187delinsTTTG
ENST00000697377.2:c.3393_3396delinsTTTG	ENSP00000513286.2:p.His1132Leu
ENST00000697379.2:c.3555_3558delinsTTTG	ENSP00000513287.2:p.His1186Leu
ENST00000561514.2:c.2664_2667delinsTTTG	ENSP00000460666.2:p.His889Leu
ENST00000697374.1:c.2664_2667delinsTTTG	ENSP00000513284.1:p.His889Leu
ENST00000697375.1:n.4896_4899delinsTTTG
ENST00000697376.1:c.*184_*187delinsTTTG	ENSP00000513285.1:n.*184_*187delinsTTTG
ENST00000697377.1:c.2502_2505delinsTTTG	ENSP00000513286.1:p.His835Leu
ENST00000697378.1:n.4069_4072delinsTTTG
ENST00000697379.1:c.2664_2667delinsTTTG	ENSP00000513287.1:p.His889Leu
ENST00000697380.1:n.2753_2756delinsTTTG
ENST00000697381.1:n.2244_2247delinsTTTG
ENST00000697382.1:c.*326_*329delinsTTTG	ENSP00000513288.1:n.*326_*329delinsTTTG
ENST00000697383.1:c.1083_1086delinsTTTG	ENSP00000513289.1:p.His362Leu
ENST00000261584.9:c.3549_3552delinsTTTG MANE Select	ENSP00000261584.4:p.His1184Leu
ENST00000261584.8:c.3549_3552delinsTTTG	ENSP00000261584.4:p.His1184Leu
ENST00000566069.5:c.315_318delinsTTTG
ENST00000568219.5:c.2664_2667delinsTTTG	ENSP00000454703.2:p.His889Leu
NM_024675.3:c.3549_3552delinsTTTG , LRG_308t1:c.3549_3552delinsTTTG	NP_078951.2:p.His1184Leu
XM_011545946.1:c.3555_3558delinsTTTG	XP_011544248.1:p.His1186Leu
XM_011545947.1:c.*184_*187delinsTTTG	XP_011544249.1:n.*184_*187delinsTTTG
XM_011545948.1:c.2664_2667delinsTTTG	XP_011544250.1:p.His889Leu
XR_950851.1:n.4257_4260delinsTTTG
XM_011545946.2:c.3555_3558delinsTTTG	XP_011544248.1:p.His1186Leu
XM_011545947.2:c.*184_*187delinsTTTG	XP_011544249.1:n.*184_*187delinsTTTG
XM_011545948.2:c.2664_2667delinsTTTG	XP_011544250.1:p.His889Leu
XM_017023671.1:c.3318_3321delinsTTTG	XP_016879160.1:p.His1107Leu
XM_017023672.2:c.3312_3315delinsTTTG	XP_016879161.1:p.His1105Leu
XM_017023673.2:c.*184_*187delinsTTTG	XP_016879162.1:n.*184_*187delinsTTTG
NM_024675.4:c.3549_3552delinsTTTG MANE Select	NP_078951.2:p.His1184Leu