Canonical Allele Identifier: CA2213424214

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603421A= , CM000678.2:g.23603421A=	GRCh38
NC_000016.9:g.23614742A= , CM000678.1:g.23614742A=	GRCh37
NC_000016.8:g.23522243A=	NCBI36
NG_007406.1:g.42937T= , LRG_308:g.42937T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.*38T=	ENSP00000460666.3:n.*38T=
ENST00000565038.2:c.*1084T=	ENSP00000459882.2:n.*1084T=
ENST00000566069.6:c.*234T=	ENSP00000459237.2:n.*234T=
ENST00000697377.2:c.*38T=	ENSP00000513286.2:n.*38T=
ENST00000697379.2:c.*38T=	ENSP00000513287.2:n.*38T=
ENST00000561514.2:c.*38T=	ENSP00000460666.2:n.*38T=
ENST00000697374.1:c.*38T=	ENSP00000513284.1:n.*38T=
ENST00000697375.1:n.4946T=
ENST00000697376.1:c.*234T=	ENSP00000513285.1:n.*234T=
ENST00000697377.1:c.*38T=	ENSP00000513286.1:n.*38T=
ENST00000697378.1:n.4119T=
ENST00000697379.1:c.*38T=	ENSP00000513287.1:n.*38T=
ENST00000697380.1:n.2803T=
ENST00000697381.1:n.2294T=
ENST00000697382.1:c.*376T=	ENSP00000513288.1:n.*376T=
ENST00000697383.1:c.*38T=	ENSP00000513289.1:n.*38T=
ENST00000261584.9:c.*38T= MANE Select	ENSP00000261584.4:n.*38T=
ENST00000261584.8:c.*38T=	ENSP00000261584.4:n.*38T=
ENST00000566069.5:c.365T=
ENST00000568219.5:c.*38T=	ENSP00000454703.2:n.*38T=
NM_024675.3:c.*38T= , LRG_308t1:c.*38T=	NP_078951.2:n.*38T=
XM_011545946.1:c.*38T=	XP_011544248.1:n.*38T=
XM_011545947.1:c.*234T=	XP_011544249.1:n.*234T=
XM_011545948.1:c.*38T=	XP_011544250.1:n.*38T=
XR_950851.1:n.4307T=
XM_011545946.2:c.*38T=	XP_011544248.1:n.*38T=
XM_011545947.2:c.*234T=	XP_011544249.1:n.*234T=
XM_011545948.2:c.*38T=	XP_011544250.1:n.*38T=
XM_017023671.1:c.*38T=	XP_016879160.1:n.*38T=
XM_017023672.2:c.*38T=	XP_016879161.1:n.*38T=
XM_017023673.2:c.*234T=	XP_016879162.1:n.*234T=
NM_024675.4:c.*38T= MANE Select	NP_078951.2:n.*38T=