Canonical Allele Identifier: CA2213431825

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636080T= , CM000678.2:g.23636080T=	GRCh38
NC_000016.9:g.23647401T= , CM000678.1:g.23647401T=	GRCh37
NC_000016.8:g.23554902T=	NCBI36
NG_007406.1:g.10278A= , LRG_308:g.10278A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.472A=	ENSP00000460666.3:p.Ile158=
ENST00000565038.2:c.211+1770A=	ENSP00000459882.2:n.211+1770A=
ENST00000566069.6:c.466A=	ENSP00000459237.2:p.Ile156=
ENST00000697377.2:c.472A=	ENSP00000513286.2:p.Ile158=
ENST00000697379.2:c.472A=	ENSP00000513287.2:p.Ile158=
ENST00000561514.2:c.-420A=	ENSP00000460666.2:n.-420A=
ENST00000697374.1:c.-420A=	ENSP00000513284.1:n.-420A=
ENST00000697375.1:n.1813A=
ENST00000697376.1:c.-420A=	ENSP00000513285.1:n.-420A=
ENST00000697377.1:c.-420A=	ENSP00000513286.1:n.-420A=
ENST00000697378.1:n.986A=
ENST00000697379.1:c.-420A=	ENSP00000513287.1:n.-420A=
ENST00000697382.1:c.-420A=	ENSP00000513288.1:n.-420A=
ENST00000697383.1:c.48+5030A=	ENSP00000513289.1:n.48+5030A=
ENST00000697384.1:n.620A=
ENST00000261584.9:c.466A= MANE Select	ENSP00000261584.4:p.Ile156=
ENST00000261584.8:c.466A=	ENSP00000261584.4:p.Ile156=
ENST00000565038.1:c.86+1770A=
ENST00000567003.1:n.744A=
ENST00000568219.5:c.-420A=	ENSP00000454703.2:n.-420A=
NM_024675.3:c.466A= , LRG_308t1:c.466A=	NP_078951.2:p.Ile156=
XM_011545946.1:c.472A=	XP_011544248.1:p.Ile158=
XM_011545947.1:c.472A=	XP_011544249.1:p.Ile158=
XM_011545948.1:c.-420A=	XP_011544250.1:n.-420A=
XR_950851.1:n.1262A=
XM_011545946.2:c.472A=	XP_011544248.1:p.Ile158=
XM_011545947.2:c.472A=	XP_011544249.1:p.Ile158=
XM_011545948.2:c.-420A=	XP_011544250.1:n.-420A=
XM_017023671.1:c.472A=	XP_016879160.1:p.Ile158=
XM_017023672.2:c.466A=	XP_016879161.1:p.Ile156=
XM_017023673.2:c.466A=	XP_016879162.1:p.Ile156=
NM_024675.4:c.466A= MANE Select	NP_078951.2:p.Ile156=