Canonical Allele Identifier: CA2213424428

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603571A= , CM000678.2:g.23603571A=	GRCh38
NC_000016.9:g.23614892A= , CM000678.1:g.23614892A=	GRCh37
NC_000016.8:g.23522393A=	NCBI36
NG_007406.1:g.42787T= , LRG_308:g.42787T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3455T=	ENSP00000460666.3:p.Leu1152=
ENST00000565038.2:c.*934T=	ENSP00000459882.2:n.*934T=
ENST00000566069.6:c.*84T=	ENSP00000459237.2:n.*84T=
ENST00000697377.2:c.3293T=	ENSP00000513286.2:p.Leu1098=
ENST00000697379.2:c.3455T=	ENSP00000513287.2:p.Leu1152=
ENST00000561514.2:c.2564T=	ENSP00000460666.2:p.Leu855=
ENST00000697374.1:c.2564T=	ENSP00000513284.1:p.Leu855=
ENST00000697375.1:n.4796T=
ENST00000697376.1:c.*84T=	ENSP00000513285.1:n.*84T=
ENST00000697377.1:c.2402T=	ENSP00000513286.1:p.Leu801=
ENST00000697378.1:n.3969T=
ENST00000697379.1:c.2564T=	ENSP00000513287.1:p.Leu855=
ENST00000697380.1:n.2653T=
ENST00000697381.1:n.2144T=
ENST00000697382.1:c.*226T=	ENSP00000513288.1:n.*226T=
ENST00000697383.1:c.983T=	ENSP00000513289.1:p.Leu328=
ENST00000261584.9:c.3449T= MANE Select	ENSP00000261584.4:p.Leu1150=
ENST00000261584.8:c.3449T=	ENSP00000261584.4:p.Leu1150=
ENST00000566069.5:c.215T=
ENST00000568219.5:c.2564T=	ENSP00000454703.2:p.Leu855=
NM_024675.3:c.3449T= , LRG_308t1:c.3449T=	NP_078951.2:p.Leu1150=
XM_011545946.1:c.3455T=	XP_011544248.1:p.Leu1152=
XM_011545947.1:c.*84T=	XP_011544249.1:n.*84T=
XM_011545948.1:c.2564T=	XP_011544250.1:p.Leu855=
XR_950851.1:n.4157T=
XM_011545946.2:c.3455T=	XP_011544248.1:p.Leu1152=
XM_011545947.2:c.*84T=	XP_011544249.1:n.*84T=
XM_011545948.2:c.2564T=	XP_011544250.1:p.Leu855=
XM_017023671.1:c.3218T=	XP_016879160.1:p.Leu1073=
XM_017023672.2:c.3212T=	XP_016879161.1:p.Leu1071=
XM_017023673.2:c.*84T=	XP_016879162.1:n.*84T=
NM_024675.4:c.3449T= MANE Select	NP_078951.2:p.Leu1150=