Canonical Allele Identifier: CA2213431805

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636073_23636074delinsTG , CM000678.2:g.23636073_23636074delinsTG	GRCh38
NC_000016.9:g.23647394_23647395delinsTG , CM000678.1:g.23647394_23647395delinsTG	GRCh37
NC_000016.8:g.23554895_23554896delinsTG	NCBI36
NG_007406.1:g.10284_10285delinsCA , LRG_308:g.10284_10285delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.478_479delinsCA	ENSP00000460666.3:p.Gln160=
ENST00000565038.2:c.211+1776_211+1777delinsCA	ENSP00000459882.2:n.211+1776_211+1777delinsCA
ENST00000566069.6:c.472_473delinsCA	ENSP00000459237.2:p.Gln158=
ENST00000697377.2:c.478_479delinsCA	ENSP00000513286.2:p.Gln160=
ENST00000697379.2:c.478_479delinsCA	ENSP00000513287.2:p.Gln160=
ENST00000561514.2:c.-414_-413delinsCA	ENSP00000460666.2:n.-414_-413delinsCA
ENST00000697374.1:c.-414_-413delinsCA	ENSP00000513284.1:n.-414_-413delinsCA
ENST00000697375.1:n.1819_1820delinsCA
ENST00000697376.1:c.-414_-413delinsCA	ENSP00000513285.1:n.-414_-413delinsCA
ENST00000697377.1:c.-414_-413delinsCA	ENSP00000513286.1:n.-414_-413delinsCA
ENST00000697378.1:n.992_993delinsCA
ENST00000697379.1:c.-414_-413delinsCA	ENSP00000513287.1:n.-414_-413delinsCA
ENST00000697382.1:c.-414_-413delinsCA	ENSP00000513288.1:n.-414_-413delinsCA
ENST00000697383.1:c.48+5036_48+5037delinsCA	ENSP00000513289.1:n.48+5036_48+5037delinsCA
ENST00000697384.1:n.626_627delinsCA
ENST00000261584.9:c.472_473delinsCA MANE Select	ENSP00000261584.4:p.Gln158=
ENST00000261584.8:c.472_473delinsCA	ENSP00000261584.4:p.Gln158=
ENST00000565038.1:c.86+1776_86+1777delinsCA
ENST00000567003.1:n.750_751delinsCA
ENST00000568219.5:c.-414_-413delinsCA	ENSP00000454703.2:n.-414_-413delinsCA
NM_024675.3:c.472_473delinsCA , LRG_308t1:c.472_473delinsCA	NP_078951.2:p.Gln158=
XM_011545946.1:c.478_479delinsCA	XP_011544248.1:p.Gln160=
XM_011545947.1:c.478_479delinsCA	XP_011544249.1:p.Gln160=
XM_011545948.1:c.-414_-413delinsCA	XP_011544250.1:n.-414_-413delinsCA
XR_950851.1:n.1268_1269delinsCA
XM_011545946.2:c.478_479delinsCA	XP_011544248.1:p.Gln160=
XM_011545947.2:c.478_479delinsCA	XP_011544249.1:p.Gln160=
XM_011545948.2:c.-414_-413delinsCA	XP_011544250.1:n.-414_-413delinsCA
XM_017023671.1:c.478_479delinsCA	XP_016879160.1:p.Gln160=
XM_017023672.2:c.472_473delinsCA	XP_016879161.1:p.Gln158=
XM_017023673.2:c.472_473delinsCA	XP_016879162.1:p.Gln158=
NM_024675.4:c.472_473delinsCA MANE Select	NP_078951.2:p.Gln158=