Canonical Allele Identifier: CA2213432450

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614004C= , CM000678.2:g.23614004C=	GRCh38
NC_000016.9:g.23625325C= , CM000678.1:g.23625325C=	GRCh37
NC_000016.8:g.23532826C=	NCBI36
NG_007406.1:g.32354G= , LRG_308:g.32354G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3207G=	ENSP00000460666.3:p.Met1069=
ENST00000565038.2:c.*682G=	ENSP00000459882.2:n.*682G=
ENST00000566069.6:c.3201G=	ENSP00000459237.2:p.Met1067=
ENST00000697377.2:c.3045G=	ENSP00000513286.2:p.Met1015=
ENST00000697379.2:c.3207G=	ENSP00000513287.2:p.Met1069=
ENST00000561514.2:c.2316G=	ENSP00000460666.2:p.Met772=
ENST00000697374.1:c.2316G=	ENSP00000513284.1:p.Met772=
ENST00000697375.1:n.4548G=
ENST00000697376.1:c.2316G=	ENSP00000513285.1:p.Met772=
ENST00000697377.1:c.2154G=	ENSP00000513286.1:p.Met718=
ENST00000697378.1:n.3721G=
ENST00000697379.1:c.2316G=	ENSP00000513287.1:p.Met772=
ENST00000697380.1:n.2406-5992G=
ENST00000697381.1:n.1896G=
ENST00000697382.1:c.2229-5992G=	ENSP00000513288.1:n.2229-5992G=
ENST00000697383.1:c.735G=	ENSP00000513289.1:p.Met245=
ENST00000261584.9:c.3201G= MANE Select	ENSP00000261584.4:p.Met1067=
ENST00000261584.8:c.3201G=	ENSP00000261584.4:p.Met1067=
ENST00000566069.5:c.116G=
ENST00000568219.5:c.2316G=	ENSP00000454703.2:p.Met772=
NM_024675.3:c.3201G= , LRG_308t1:c.3201G=	NP_078951.2:p.Met1067=
XM_011545946.1:c.3207G=	XP_011544248.1:p.Met1069=
XM_011545947.1:c.3207G=	XP_011544249.1:p.Met1069=
XM_011545948.1:c.2316G=	XP_011544250.1:p.Met772=
XR_950851.1:n.3910-5992G=
XM_011545946.2:c.3207G=	XP_011544248.1:p.Met1069=
XM_011545947.2:c.3207G=	XP_011544249.1:p.Met1069=
XM_011545948.2:c.2316G=	XP_011544250.1:p.Met772=
XM_017023671.1:c.3119+7358G=	XP_016879160.1:n.3119+7358G=
XM_017023672.2:c.3113+7358G=	XP_016879161.1:n.3113+7358G=
XM_017023673.2:c.3201G=	XP_016879162.1:p.Met1067=
NM_024675.4:c.3201G= MANE Select	NP_078951.2:p.Met1067=