Canonical Allele Identifier: CA2213432181

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636203C= , CM000678.2:g.23636203C=	GRCh38
NC_000016.9:g.23647524C= , CM000678.1:g.23647524C=	GRCh37
NC_000016.8:g.23555025C=	NCBI36
NG_007406.1:g.10155G= , LRG_308:g.10155G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.349G=	ENSP00000460666.3:p.Gly117=
ENST00000565038.2:c.211+1647G=	ENSP00000459882.2:n.211+1647G=
ENST00000566069.6:c.343G=	ENSP00000459237.2:p.Gly115=
ENST00000697377.2:c.349G=	ENSP00000513286.2:p.Gly117=
ENST00000697379.2:c.349G=	ENSP00000513287.2:p.Gly117=
ENST00000561514.2:c.-543G=	ENSP00000460666.2:n.-543G=
ENST00000697374.1:c.-543G=	ENSP00000513284.1:n.-543G=
ENST00000697375.1:n.1690G=
ENST00000697376.1:c.-543G=	ENSP00000513285.1:n.-543G=
ENST00000697377.1:c.-543G=	ENSP00000513286.1:n.-543G=
ENST00000697378.1:n.863G=
ENST00000697379.1:c.-543G=	ENSP00000513287.1:n.-543G=
ENST00000697382.1:c.-543G=	ENSP00000513288.1:n.-543G=
ENST00000697383.1:c.48+4907G=	ENSP00000513289.1:n.48+4907G=
ENST00000697384.1:n.497G=
ENST00000261584.9:c.343G= MANE Select	ENSP00000261584.4:p.Gly115=
ENST00000261584.8:c.343G=	ENSP00000261584.4:p.Gly115=
ENST00000565038.1:c.86+1647G=
ENST00000567003.1:n.621G=
ENST00000568219.5:c.-543G=	ENSP00000454703.2:n.-543G=
NM_024675.3:c.343G= , LRG_308t1:c.343G=	NP_078951.2:p.Gly115=
XM_011545946.1:c.349G=	XP_011544248.1:p.Gly117=
XM_011545947.1:c.349G=	XP_011544249.1:p.Gly117=
XM_011545948.1:c.-543G=	XP_011544250.1:n.-543G=
XR_950851.1:n.1139G=
XM_011545946.2:c.349G=	XP_011544248.1:p.Gly117=
XM_011545947.2:c.349G=	XP_011544249.1:p.Gly117=
XM_011545948.2:c.-543G=	XP_011544250.1:n.-543G=
XM_017023671.1:c.349G=	XP_016879160.1:p.Gly117=
XM_017023672.2:c.343G=	XP_016879161.1:p.Gly115=
XM_017023673.2:c.343G=	XP_016879162.1:p.Gly115=
NM_024675.4:c.343G= MANE Select	NP_078951.2:p.Gly115=