Canonical Allele Identifier: CA2213436427

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641122_23641123delinsCT , CM000678.2:g.23641122_23641123delinsCT	GRCh38
NC_000016.9:g.23652443_23652444delinsCT , CM000678.1:g.23652443_23652444delinsCT	GRCh37
NC_000016.8:g.23559944_23559945delinsCT	NCBI36
NG_007406.1:g.5235_5236delinsAG , LRG_308:g.5235_5236delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-818_-817delinsAG	ENSP00000460666.3:n.-818_-817delinsAG
ENST00000565038.2:c.35_36delinsAG	ENSP00000459882.2:p.Glu12=
ENST00000566069.6:c.35_36delinsAG	ENSP00000459237.2:p.Glu12=
ENST00000697377.2:c.-205_-204delinsAG	ENSP00000513286.2:n.-205_-204delinsAG
ENST00000697379.2:c.-111_-110delinsAG	ENSP00000513287.2:n.-111_-110delinsAG
ENST00000561514.2:c.-1709_-1708delinsAG	ENSP00000460666.2:n.-1709_-1708delinsAG
ENST00000697374.1:c.-1300_-1299delinsAG	ENSP00000513284.1:n.-1300_-1299delinsAG
ENST00000697376.1:c.-1021_-1020delinsAG	ENSP00000513285.1:n.-1021_-1020delinsAG
ENST00000697377.1:c.-1096_-1095delinsAG	ENSP00000513286.1:n.-1096_-1095delinsAG
ENST00000697379.1:c.-1002_-1001delinsAG	ENSP00000513287.1:n.-1002_-1001delinsAG
ENST00000697382.1:c.-1760_-1759delinsAG	ENSP00000513288.1:n.-1760_-1759delinsAG
ENST00000697383.1:c.35_36delinsAG	ENSP00000513289.1:p.Glu12=
ENST00000697384.1:n.189_190delinsAG
ENST00000261584.9:c.35_36delinsAG MANE Select	ENSP00000261584.4:p.Glu12=
ENST00000261584.8:c.35_36delinsAG	ENSP00000261584.4:p.Glu12=
ENST00000567003.1:n.179_180delinsAG
ENST00000568219.5:c.-838+4_-838+5delinsAG	ENSP00000454703.2:n.-838+4_-838+5delinsAG
NM_024675.3:c.35_36delinsAG , LRG_308t1:c.35_36delinsAG	NP_078951.2:p.Glu12=
XM_011545948.1:c.-985_-984delinsAG	XP_011544250.1:n.-985_-984delinsAG
XM_011545946.2:c.-818_-817delinsAG	XP_011544248.1:n.-818_-817delinsAG
XM_011545947.2:c.-818_-817delinsAG	XP_011544249.1:n.-818_-817delinsAG
XM_011545948.2:c.-985_-984delinsAG	XP_011544250.1:n.-985_-984delinsAG
XM_017023671.1:c.-818_-817delinsAG	XP_016879160.1:n.-818_-817delinsAG
XM_017023672.2:c.35_36delinsAG	XP_016879161.1:p.Glu12=
XM_017023673.2:c.35_36delinsAG	XP_016879162.1:p.Glu12=
NM_024675.4:c.35_36delinsAG MANE Select	NP_078951.2:p.Glu12=