Canonical Allele Identifier: CA2213415285

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624098A= , CM000678.2:g.23624098A=	GRCh38
NC_000016.9:g.23635419A= , CM000678.1:g.23635419A=	GRCh37
NC_000016.8:g.23542920A=	NCBI36
NG_007406.1:g.22260T= , LRG_308:g.22260T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2755-4T=	ENSP00000460666.3:n.2755-4T=
ENST00000565038.2:c.*230-4T=	ENSP00000459882.2:n.*230-4T=
ENST00000566069.6:c.2749-4T=	ENSP00000459237.2:n.2749-4T=
ENST00000697377.2:c.2593-4T=	ENSP00000513286.2:n.2593-4T=
ENST00000697379.2:c.2755-4T=	ENSP00000513287.2:n.2755-4T=
ENST00000561514.2:c.1864-4T=	ENSP00000460666.2:n.1864-4T=
ENST00000697374.1:c.1864-4T=	ENSP00000513284.1:n.1864-4T=
ENST00000697375.1:n.4096-4T=
ENST00000697376.1:c.1864-4T=	ENSP00000513285.1:n.1864-4T=
ENST00000697377.1:c.1702-4T=	ENSP00000513286.1:n.1702-4T=
ENST00000697378.1:n.3269-4T=
ENST00000697379.1:c.1864-4T=	ENSP00000513287.1:n.1864-4T=
ENST00000697380.1:n.2041-4T=
ENST00000697381.1:n.1444-4T=
ENST00000697382.1:c.1864-4T=	ENSP00000513288.1:n.1864-4T=
ENST00000697383.1:c.283-4T=	ENSP00000513289.1:n.283-4T=
ENST00000261584.9:c.2749-4T= MANE Select	ENSP00000261584.4:n.2749-4T=
ENST00000261584.8:c.2749-4T=	ENSP00000261584.4:n.2749-4T=
ENST00000565038.1:c.321-4T=
ENST00000568219.5:c.1864-4T=	ENSP00000454703.2:n.1864-4T=
NM_024675.3:c.2749-4T= , LRG_308t1:c.2749-4T=	NP_078951.2:n.2749-4T=
XM_011545946.1:c.2755-4T=	XP_011544248.1:n.2755-4T=
XM_011545947.1:c.2755-4T=	XP_011544249.1:n.2755-4T=
XM_011545948.1:c.1864-4T=	XP_011544250.1:n.1864-4T=
XR_950851.1:n.3545-4T=
XM_011545946.2:c.2755-4T=	XP_011544248.1:n.2755-4T=
XM_011545947.2:c.2755-4T=	XP_011544249.1:n.2755-4T=
XM_011545948.2:c.1864-4T=	XP_011544250.1:n.1864-4T=
XM_017023671.1:c.2755-4T=	XP_016879160.1:n.2755-4T=
XM_017023672.2:c.2749-4T=	XP_016879161.1:n.2749-4T=
XM_017023673.2:c.2749-4T=	XP_016879162.1:n.2749-4T=
NM_024675.4:c.2749-4T= MANE Select	NP_078951.2:n.2749-4T=