Canonical Allele Identifier: CA3217598484

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603594T= , CM000678.2:g.23603594T=	GRCh38
NC_000016.9:g.23614915T= , CM000678.1:g.23614915T=	GRCh37
NC_000016.8:g.23522416T=	NCBI36
NG_007406.1:g.42764A= , LRG_308:g.42764A=

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.3426A= MANE Select	NP_078951.2:p.Leu1142=
ENST00000261584.9:c.3426A= MANE Select	ENSP00000261584.4:p.Leu1142=
NM_024675.3:c.3426A= , LRG_308t1:c.3426A=	NP_078951.2:p.Leu1142=
ENST00000261584.8:c.3426A=	ENSP00000261584.4:p.Leu1142=
ENST00000561514.2:c.2541A=	ENSP00000460666.2:p.Leu847=
ENST00000561514.3:c.3432A=	ENSP00000460666.3:p.Leu1144=
ENST00000565038.2:c.*911A=	ENSP00000459882.2:n.*911A=
ENST00000566069.5:c.192A=
ENST00000566069.6:c.*61A=	ENSP00000459237.2:n.*61A=
ENST00000568219.5:c.2541A=	ENSP00000454703.2:p.Leu847=
ENST00000697374.1:c.2541A=	ENSP00000513284.1:p.Leu847=
ENST00000697375.1:n.4773A=
ENST00000697376.1:c.*61A=	ENSP00000513285.1:n.*61A=
ENST00000697377.1:c.2379A=	ENSP00000513286.1:p.Leu793=
ENST00000697377.2:c.3270A=	ENSP00000513286.2:p.Leu1090=
ENST00000697378.1:n.3946A=
ENST00000697379.1:c.2541A=	ENSP00000513287.1:p.Leu847=
ENST00000697379.2:c.3432A=	ENSP00000513287.2:p.Leu1144=
ENST00000697380.1:n.2630A=
ENST00000697381.1:n.2121A=
ENST00000697382.1:c.*203A=	ENSP00000513288.1:n.*203A=
ENST00000697383.1:c.960A=	ENSP00000513289.1:p.Leu320=
XM_011545946.1:c.3432A=	XP_011544248.1:p.Leu1144=
XM_011545946.2:c.3432A=	XP_011544248.1:p.Leu1144=
XM_011545947.1:c.*61A=	XP_011544249.1:n.*61A=
XM_011545947.2:c.*61A=	XP_011544249.1:n.*61A=
XM_011545948.1:c.2541A=	XP_011544250.1:p.Leu847=
XM_011545948.2:c.2541A=	XP_011544250.1:p.Leu847=
XM_017023671.1:c.3195A=	XP_016879160.1:p.Leu1065=
XM_017023672.2:c.3189A=	XP_016879161.1:p.Leu1063=
XM_017023673.2:c.*61A=	XP_016879162.1:n.*61A=
XR_950851.1:n.4134A=