Canonical Allele Identifier: CA2213432136

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636190_23636191delinsTG , CM000678.2:g.23636190_23636191delinsTG	GRCh38
NC_000016.9:g.23647511_23647512delinsTG , CM000678.1:g.23647511_23647512delinsTG	GRCh37
NC_000016.8:g.23555012_23555013delinsTG	NCBI36
NG_007406.1:g.10167_10168delinsCA , LRG_308:g.10167_10168delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.361_362delinsCA	ENSP00000460666.3:p.Gln121=
ENST00000565038.2:c.211+1659_211+1660delinsCA	ENSP00000459882.2:n.211+1659_211+1660delinsCA
ENST00000566069.6:c.355_356delinsCA	ENSP00000459237.2:p.Gln119=
ENST00000697377.2:c.361_362delinsCA	ENSP00000513286.2:p.Gln121=
ENST00000697379.2:c.361_362delinsCA	ENSP00000513287.2:p.Gln121=
ENST00000561514.2:c.-531_-530delinsCA	ENSP00000460666.2:n.-531_-530delinsCA
ENST00000697374.1:c.-531_-530delinsCA	ENSP00000513284.1:n.-531_-530delinsCA
ENST00000697375.1:n.1702_1703delinsCA
ENST00000697376.1:c.-531_-530delinsCA	ENSP00000513285.1:n.-531_-530delinsCA
ENST00000697377.1:c.-531_-530delinsCA	ENSP00000513286.1:n.-531_-530delinsCA
ENST00000697378.1:n.875_876delinsCA
ENST00000697379.1:c.-531_-530delinsCA	ENSP00000513287.1:n.-531_-530delinsCA
ENST00000697382.1:c.-531_-530delinsCA	ENSP00000513288.1:n.-531_-530delinsCA
ENST00000697383.1:c.48+4919_48+4920delinsCA	ENSP00000513289.1:n.48+4919_48+4920delinsCA
ENST00000697384.1:n.509_510delinsCA
ENST00000261584.9:c.355_356delinsCA MANE Select	ENSP00000261584.4:p.Gln119=
ENST00000261584.8:c.355_356delinsCA	ENSP00000261584.4:p.Gln119=
ENST00000565038.1:c.86+1659_86+1660delinsCA
ENST00000567003.1:n.633_634delinsCA
ENST00000568219.5:c.-531_-530delinsCA	ENSP00000454703.2:n.-531_-530delinsCA
NM_024675.3:c.355_356delinsCA , LRG_308t1:c.355_356delinsCA	NP_078951.2:p.Gln119=
XM_011545946.1:c.361_362delinsCA	XP_011544248.1:p.Gln121=
XM_011545947.1:c.361_362delinsCA	XP_011544249.1:p.Gln121=
XM_011545948.1:c.-531_-530delinsCA	XP_011544250.1:n.-531_-530delinsCA
XR_950851.1:n.1151_1152delinsCA
XM_011545946.2:c.361_362delinsCA	XP_011544248.1:p.Gln121=
XM_011545947.2:c.361_362delinsCA	XP_011544249.1:p.Gln121=
XM_011545948.2:c.-531_-530delinsCA	XP_011544250.1:n.-531_-530delinsCA
XM_017023671.1:c.361_362delinsCA	XP_016879160.1:p.Gln121=
XM_017023672.2:c.355_356delinsCA	XP_016879161.1:p.Gln119=
XM_017023673.2:c.355_356delinsCA	XP_016879162.1:p.Gln119=
NM_024675.4:c.355_356delinsCA MANE Select	NP_078951.2:p.Gln119=