Canonical Allele Identifier: CA2213434188

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23638002_23638004delinsTAG , CM000678.2:g.23638002_23638004delinsTAG	GRCh38
NC_000016.9:g.23649323_23649325delinsTAG , CM000678.1:g.23649323_23649325delinsTAG	GRCh37
NC_000016.8:g.23556824_23556826delinsTAG	NCBI36
NG_007406.1:g.8354_8356delinsCTA , LRG_308:g.8354_8356delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.115-52_115-50delinsCTA	ENSP00000460666.3:n.115-52_115-50delinsCTA
ENST00000565038.2:c.109-52_109-50delinsCTA	ENSP00000459882.2:n.109-52_109-50delinsCTA
ENST00000566069.6:c.109-52_109-50delinsCTA	ENSP00000459237.2:n.109-52_109-50delinsCTA
ENST00000697377.2:c.115-52_115-50delinsCTA	ENSP00000513286.2:n.115-52_115-50delinsCTA
ENST00000697379.2:c.115-52_115-50delinsCTA	ENSP00000513287.2:n.115-52_115-50delinsCTA
ENST00000561514.2:c.-777-52_-777-50delinsCTA	ENSP00000460666.2:n.-777-52_-777-50delinsCTA
ENST00000697374.1:c.-777-52_-777-50delinsCTA	ENSP00000513284.1:n.-777-52_-777-50delinsCTA
ENST00000697375.1:n.1456-52_1456-50delinsCTA
ENST00000697376.1:c.-813-16_-813-14delinsCTA	ENSP00000513285.1:n.-813-16_-813-14delinsCTA
ENST00000697377.1:c.-777-52_-777-50delinsCTA	ENSP00000513286.1:n.-777-52_-777-50delinsCTA
ENST00000697378.1:n.629-52_629-50delinsCTA
ENST00000697379.1:c.-777-52_-777-50delinsCTA	ENSP00000513287.1:n.-777-52_-777-50delinsCTA
ENST00000697382.1:c.-777-52_-777-50delinsCTA	ENSP00000513288.1:n.-777-52_-777-50delinsCTA
ENST00000697383.1:c.48+3106_48+3108delinsCTA	ENSP00000513289.1:n.48+3106_48+3108delinsCTA
ENST00000697384.1:n.263-52_263-50delinsCTA
ENST00000261584.9:c.109-52_109-50delinsCTA MANE Select	ENSP00000261584.4:n.109-52_109-50delinsCTA
ENST00000261584.8:c.109-52_109-50delinsCTA	ENSP00000261584.4:n.109-52_109-50delinsCTA
ENST00000561514.1:c.115-52_115-50delinsCTA	ENSP00000460666.1:n.115-52_115-50delinsCTA
ENST00000567003.1:n.387-52_387-50delinsCTA
ENST00000568219.5:c.-777-52_-777-50delinsCTA	ENSP00000454703.2:n.-777-52_-777-50delinsCTA
NM_024675.3:c.109-52_109-50delinsCTA , LRG_308t1:c.109-52_109-50delinsCTA	NP_078951.2:n.109-52_109-50delinsCTA
XM_011545946.1:c.115-52_115-50delinsCTA	XP_011544248.1:n.115-52_115-50delinsCTA
XM_011545947.1:c.115-52_115-50delinsCTA	XP_011544249.1:n.115-52_115-50delinsCTA
XM_011545948.1:c.-777-52_-777-50delinsCTA	XP_011544250.1:n.-777-52_-777-50delinsCTA
XR_950851.1:n.905-52_905-50delinsCTA
XM_011545946.2:c.115-52_115-50delinsCTA	XP_011544248.1:n.115-52_115-50delinsCTA
XM_011545947.2:c.115-52_115-50delinsCTA	XP_011544249.1:n.115-52_115-50delinsCTA
XM_011545948.2:c.-777-52_-777-50delinsCTA	XP_011544250.1:n.-777-52_-777-50delinsCTA
XM_017023671.1:c.115-52_115-50delinsCTA	XP_016879160.1:n.115-52_115-50delinsCTA
XM_017023672.2:c.109-52_109-50delinsCTA	XP_016879161.1:n.109-52_109-50delinsCTA
XM_017023673.2:c.109-52_109-50delinsCTA	XP_016879162.1:n.109-52_109-50delinsCTA
NM_024675.4:c.109-52_109-50delinsCTA MANE Select	NP_078951.2:n.109-52_109-50delinsCTA