Canonical Allele Identifier: CA2213424267

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603473A= , CM000678.2:g.23603473A=	GRCh38
NC_000016.9:g.23614794A= , CM000678.1:g.23614794A=	GRCh37
NC_000016.8:g.23522295A=	NCBI36
NG_007406.1:g.42885T= , LRG_308:g.42885T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3553T=	ENSP00000460666.3:p.Tyr1185=
ENST00000565038.2:c.*1032T=	ENSP00000459882.2:n.*1032T=
ENST00000566069.6:c.*182T=	ENSP00000459237.2:n.*182T=
ENST00000697377.2:c.3391T=	ENSP00000513286.2:p.Tyr1131=
ENST00000697379.2:c.3553T=	ENSP00000513287.2:p.Tyr1185=
ENST00000561514.2:c.2662T=	ENSP00000460666.2:p.Tyr888=
ENST00000697374.1:c.2662T=	ENSP00000513284.1:p.Tyr888=
ENST00000697375.1:n.4894T=
ENST00000697376.1:c.*182T=	ENSP00000513285.1:n.*182T=
ENST00000697377.1:c.2500T=	ENSP00000513286.1:p.Tyr834=
ENST00000697378.1:n.4067T=
ENST00000697379.1:c.2662T=	ENSP00000513287.1:p.Tyr888=
ENST00000697380.1:n.2751T=
ENST00000697381.1:n.2242T=
ENST00000697382.1:c.*324T=	ENSP00000513288.1:n.*324T=
ENST00000697383.1:c.1081T=	ENSP00000513289.1:p.Tyr361=
ENST00000261584.9:c.3547T= MANE Select	ENSP00000261584.4:p.Tyr1183=
ENST00000261584.8:c.3547T=	ENSP00000261584.4:p.Tyr1183=
ENST00000566069.5:c.313T=
ENST00000568219.5:c.2662T=	ENSP00000454703.2:p.Tyr888=
NM_024675.3:c.3547T= , LRG_308t1:c.3547T=	NP_078951.2:p.Tyr1183=
XM_011545946.1:c.3553T=	XP_011544248.1:p.Tyr1185=
XM_011545947.1:c.*182T=	XP_011544249.1:n.*182T=
XM_011545948.1:c.2662T=	XP_011544250.1:p.Tyr888=
XR_950851.1:n.4255T=
XM_011545946.2:c.3553T=	XP_011544248.1:p.Tyr1185=
XM_011545947.2:c.*182T=	XP_011544249.1:n.*182T=
XM_011545948.2:c.2662T=	XP_011544250.1:p.Tyr888=
XM_017023671.1:c.3316T=	XP_016879160.1:p.Tyr1106=
XM_017023672.2:c.3310T=	XP_016879161.1:p.Tyr1104=
XM_017023673.2:c.*182T=	XP_016879162.1:n.*182T=
NM_024675.4:c.3547T= MANE Select	NP_078951.2:p.Tyr1183=