Canonical Allele Identifier: CA2213427814

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635027_23635028delinsCT , CM000678.2:g.23635027_23635028delinsCT	GRCh38
NC_000016.9:g.23646348_23646349delinsCT , CM000678.1:g.23646348_23646349delinsCT	GRCh37
NC_000016.8:g.23553849_23553850delinsCT	NCBI36
NG_007406.1:g.11330_11331delinsAG , LRG_308:g.11330_11331delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1524_1525delinsAG	ENSP00000460666.3:p.Gln508=
ENST00000565038.2:c.211+2822_211+2823delinsAG	ENSP00000459882.2:n.211+2822_211+2823delinsAG
ENST00000566069.6:c.1518_1519delinsAG	ENSP00000459237.2:p.Gln506=
ENST00000697377.2:c.1524_1525delinsAG	ENSP00000513286.2:p.Gln508=
ENST00000697379.2:c.1524_1525delinsAG	ENSP00000513287.2:p.Gln508=
ENST00000561514.2:c.633_634delinsAG	ENSP00000460666.2:p.Gln211=
ENST00000697374.1:c.633_634delinsAG	ENSP00000513284.1:p.Gln211=
ENST00000697375.1:n.2865_2866delinsAG
ENST00000697376.1:c.633_634delinsAG	ENSP00000513285.1:p.Gln211=
ENST00000697377.1:c.633_634delinsAG	ENSP00000513286.1:p.Gln211=
ENST00000697378.1:n.2038_2039delinsAG
ENST00000697379.1:c.633_634delinsAG	ENSP00000513287.1:p.Gln211=
ENST00000697382.1:c.633_634delinsAG	ENSP00000513288.1:p.Gln211=
ENST00000697383.1:c.49-5753_49-5752delinsAG	ENSP00000513289.1:n.49-5753_49-5752delinsAG
ENST00000697384.1:n.1672_1673delinsAG
ENST00000261584.9:c.1518_1519delinsAG MANE Select	ENSP00000261584.4:p.Gln506=
ENST00000261584.8:c.1518_1519delinsAG	ENSP00000261584.4:p.Gln506=
ENST00000565038.1:c.86+2822_86+2823delinsAG
ENST00000568219.5:c.633_634delinsAG	ENSP00000454703.2:p.Gln211=
NM_024675.3:c.1518_1519delinsAG , LRG_308t1:c.1518_1519delinsAG	NP_078951.2:p.Gln506=
XM_011545946.1:c.1524_1525delinsAG	XP_011544248.1:p.Gln508=
XM_011545947.1:c.1524_1525delinsAG	XP_011544249.1:p.Gln508=
XM_011545948.1:c.633_634delinsAG	XP_011544250.1:p.Gln211=
XR_950851.1:n.2314_2315delinsAG
XM_011545946.2:c.1524_1525delinsAG	XP_011544248.1:p.Gln508=
XM_011545947.2:c.1524_1525delinsAG	XP_011544249.1:p.Gln508=
XM_011545948.2:c.633_634delinsAG	XP_011544250.1:p.Gln211=
XM_017023671.1:c.1524_1525delinsAG	XP_016879160.1:p.Gln508=
XM_017023672.2:c.1518_1519delinsAG	XP_016879161.1:p.Gln506=
XM_017023673.2:c.1518_1519delinsAG	XP_016879162.1:p.Gln506=
NM_024675.4:c.1518_1519delinsAG MANE Select	NP_078951.2:p.Gln506=