Canonical Allele Identifier: CA2213429028

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635389_23635390delinsGT , CM000678.2:g.23635389_23635390delinsGT	GRCh38
NC_000016.9:g.23646710_23646711delinsGT , CM000678.1:g.23646710_23646711delinsGT	GRCh37
NC_000016.8:g.23554211_23554212delinsGT	NCBI36
NG_007406.1:g.10968_10969delinsAC , LRG_308:g.10968_10969delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1162_1163delinsAC	ENSP00000460666.3:p.Thr388=
ENST00000565038.2:c.211+2460_211+2461delinsAC	ENSP00000459882.2:n.211+2460_211+2461deli...
ENST00000566069.6:c.1156_1157delinsAC	ENSP00000459237.2:p.Thr386=
ENST00000697377.2:c.1162_1163delinsAC	ENSP00000513286.2:p.Thr388=
ENST00000697379.2:c.1162_1163delinsAC	ENSP00000513287.2:p.Thr388=
ENST00000561514.2:c.271_272delinsAC	ENSP00000460666.2:p.Thr91=
ENST00000697374.1:c.271_272delinsAC	ENSP00000513284.1:p.Thr91=
ENST00000697375.1:n.2503_2504delinsAC
ENST00000697376.1:c.271_272delinsAC	ENSP00000513285.1:p.Thr91=
ENST00000697377.1:c.271_272delinsAC	ENSP00000513286.1:p.Thr91=
ENST00000697378.1:n.1676_1677delinsAC
ENST00000697379.1:c.271_272delinsAC	ENSP00000513287.1:p.Thr91=
ENST00000697382.1:c.271_272delinsAC	ENSP00000513288.1:p.Thr91=
ENST00000697383.1:c.48+5720_48+5721delinsAC	ENSP00000513289.1:n.48+5720_48+5721delins...
ENST00000697384.1:n.1310_1311delinsAC
ENST00000261584.9:c.1156_1157delinsAC MANE Select	ENSP00000261584.4:p.Thr386=
ENST00000261584.8:c.1156_1157delinsAC	ENSP00000261584.4:p.Thr386=
ENST00000565038.1:c.86+2460_86+2461delinsAC
ENST00000568219.5:c.271_272delinsAC	ENSP00000454703.2:p.Thr91=
NM_024675.3:c.1156_1157delinsAC , LRG_308t1:c.1156_1157delinsAC	NP_078951.2:p.Thr386=
XM_011545946.1:c.1162_1163delinsAC	XP_011544248.1:p.Thr388=
XM_011545947.1:c.1162_1163delinsAC	XP_011544249.1:p.Thr388=
XM_011545948.1:c.271_272delinsAC	XP_011544250.1:p.Thr91=
XR_950851.1:n.1952_1953delinsAC
XM_011545946.2:c.1162_1163delinsAC	XP_011544248.1:p.Thr388=
XM_011545947.2:c.1162_1163delinsAC	XP_011544249.1:p.Thr388=
XM_011545948.2:c.271_272delinsAC	XP_011544250.1:p.Thr91=
XM_017023671.1:c.1162_1163delinsAC	XP_016879160.1:p.Thr388=
XM_017023672.2:c.1156_1157delinsAC	XP_016879161.1:p.Thr386=
XM_017023673.2:c.1156_1157delinsAC	XP_016879162.1:p.Thr386=
NM_024675.4:c.1156_1157delinsAC MANE Select	NP_078951.2:p.Thr386=