Canonical Allele Identifier: CA2213429582

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635514_23635515delinsGT , CM000678.2:g.23635514_23635515delinsGT	GRCh38
NC_000016.9:g.23646835_23646836delinsGT , CM000678.1:g.23646835_23646836delinsGT	GRCh37
NC_000016.8:g.23554336_23554337delinsGT	NCBI36
NG_007406.1:g.10843_10844delinsAC , LRG_308:g.10843_10844delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1037_1038delinsAC	ENSP00000460666.3:p.Asn346=
ENST00000565038.2:c.211+2335_211+2336delinsAC	ENSP00000459882.2:n.211+2335_211+2336delinsAC
ENST00000566069.6:c.1031_1032delinsAC	ENSP00000459237.2:p.Asn344=
ENST00000697377.2:c.1037_1038delinsAC	ENSP00000513286.2:p.Asn346=
ENST00000697379.2:c.1037_1038delinsAC	ENSP00000513287.2:p.Asn346=
ENST00000561514.2:c.146_147delinsAC	ENSP00000460666.2:p.Asn49=
ENST00000697374.1:c.146_147delinsAC	ENSP00000513284.1:p.Asn49=
ENST00000697375.1:n.2378_2379delinsAC
ENST00000697376.1:c.146_147delinsAC	ENSP00000513285.1:p.Asn49=
ENST00000697377.1:c.146_147delinsAC	ENSP00000513286.1:p.Asn49=
ENST00000697378.1:n.1551_1552delinsAC
ENST00000697379.1:c.146_147delinsAC	ENSP00000513287.1:p.Asn49=
ENST00000697382.1:c.146_147delinsAC	ENSP00000513288.1:p.Asn49=
ENST00000697383.1:c.48+5595_48+5596delinsAC	ENSP00000513289.1:n.48+5595_48+5596delinsAC
ENST00000697384.1:n.1185_1186delinsAC
ENST00000261584.9:c.1031_1032delinsAC MANE Select	ENSP00000261584.4:p.Asn344=
ENST00000261584.8:c.1031_1032delinsAC	ENSP00000261584.4:p.Asn344=
ENST00000565038.1:c.86+2335_86+2336delinsAC
ENST00000568219.5:c.146_147delinsAC	ENSP00000454703.2:p.Asn49=
NM_024675.3:c.1031_1032delinsAC , LRG_308t1:c.1031_1032delinsAC	NP_078951.2:p.Asn344=
XM_011545946.1:c.1037_1038delinsAC	XP_011544248.1:p.Asn346=
XM_011545947.1:c.1037_1038delinsAC	XP_011544249.1:p.Asn346=
XM_011545948.1:c.146_147delinsAC	XP_011544250.1:p.Asn49=
XR_950851.1:n.1827_1828delinsAC
XM_011545946.2:c.1037_1038delinsAC	XP_011544248.1:p.Asn346=
XM_011545947.2:c.1037_1038delinsAC	XP_011544249.1:p.Asn346=
XM_011545948.2:c.146_147delinsAC	XP_011544250.1:p.Asn49=
XM_017023671.1:c.1037_1038delinsAC	XP_016879160.1:p.Asn346=
XM_017023672.2:c.1031_1032delinsAC	XP_016879161.1:p.Asn344=
XM_017023673.2:c.1031_1032delinsAC	XP_016879162.1:p.Asn344=
NM_024675.4:c.1031_1032delinsAC MANE Select	NP_078951.2:p.Asn344=