Canonical Allele Identifier: CA2213409609

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621355A= , CM000678.2:g.23621355A=	GRCh38
NC_000016.9:g.23632676A= , CM000678.1:g.23632676A=	GRCh37
NC_000016.8:g.23540177A=	NCBI36
NG_007406.1:g.25003T= , LRG_308:g.25003T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3119+7T=	ENSP00000460666.3:n.3119+7T=
ENST00000565038.2:c.*594+7T=	ENSP00000459882.2:n.*594+7T=
ENST00000566069.6:c.3113+7T=	ENSP00000459237.2:n.3113+7T=
ENST00000697377.2:c.2957+7T=	ENSP00000513286.2:n.2957+7T=
ENST00000697379.2:c.3119+7T=	ENSP00000513287.2:n.3119+7T=
ENST00000561514.2:c.2228+7T=	ENSP00000460666.2:n.2228+7T=
ENST00000697374.1:c.2228+7T=	ENSP00000513284.1:n.2228+7T=
ENST00000697375.1:n.4460+7T=
ENST00000697376.1:c.2228+7T=	ENSP00000513285.1:n.2228+7T=
ENST00000697377.1:c.2066+7T=	ENSP00000513286.1:n.2066+7T=
ENST00000697378.1:n.3633+7T=
ENST00000697379.1:c.2228+7T=	ENSP00000513287.1:n.2228+7T=
ENST00000697380.1:n.2405+7T=
ENST00000697381.1:n.1808+7T=
ENST00000697382.1:c.2228+7T=	ENSP00000513288.1:n.2228+7T=
ENST00000697383.1:c.647+7T=	ENSP00000513289.1:n.647+7T=
ENST00000261584.9:c.3113+7T= MANE Select	ENSP00000261584.4:n.3113+7T=
ENST00000261584.8:c.3113+7T=	ENSP00000261584.4:n.3113+7T=
ENST00000566069.5:c.28+7T=
ENST00000568219.5:c.2228+7T=	ENSP00000454703.2:n.2228+7T=
NM_024675.3:c.3113+7T= , LRG_308t1:c.3113+7T=	NP_078951.2:n.3113+7T=
XM_011545946.1:c.3119+7T=	XP_011544248.1:n.3119+7T=
XM_011545947.1:c.3119+7T=	XP_011544249.1:n.3119+7T=
XM_011545948.1:c.2228+7T=	XP_011544250.1:n.2228+7T=
XR_950851.1:n.3909+7T=
XM_011545946.2:c.3119+7T=	XP_011544248.1:n.3119+7T=
XM_011545947.2:c.3119+7T=	XP_011544249.1:n.3119+7T=
XM_011545948.2:c.2228+7T=	XP_011544250.1:n.2228+7T=
XM_017023671.1:c.3119+7T=	XP_016879160.1:n.3119+7T=
XM_017023672.2:c.3113+7T=	XP_016879161.1:n.3113+7T=
XM_017023673.2:c.3113+7T=	XP_016879162.1:n.3113+7T=
NM_024675.4:c.3113+7T= MANE Select	NP_078951.2:n.3113+7T=