Canonical Allele Identifier: CA2213436450

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641147G= , CM000678.2:g.23641147G=	GRCh38
NC_000016.9:g.23652468G= , CM000678.1:g.23652468G=	GRCh37
NC_000016.8:g.23559969G=	NCBI36
NG_007406.1:g.5211C= , LRG_308:g.5211C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-842C=	ENSP00000460666.3:n.-842C=
ENST00000565038.2:c.11C=	ENSP00000459882.2:p.Pro4=
ENST00000566069.6:c.11C=	ENSP00000459237.2:p.Pro4=
ENST00000697377.2:c.-229C=	ENSP00000513286.2:n.-229C=
ENST00000697379.2:c.-135C=	ENSP00000513287.2:n.-135C=
ENST00000561514.2:c.-1733C=	ENSP00000460666.2:n.-1733C=
ENST00000697374.1:c.-1324C=	ENSP00000513284.1:n.-1324C=
ENST00000697376.1:c.-1045C=	ENSP00000513285.1:n.-1045C=
ENST00000697377.1:c.-1120C=	ENSP00000513286.1:n.-1120C=
ENST00000697379.1:c.-1026C=	ENSP00000513287.1:n.-1026C=
ENST00000697382.1:c.-1784C=	ENSP00000513288.1:n.-1784C=
ENST00000697383.1:c.11C=	ENSP00000513289.1:p.Pro4=
ENST00000697384.1:n.165C=
ENST00000261584.9:c.11C= MANE Select	ENSP00000261584.4:p.Pro4=
ENST00000261584.8:c.11C=	ENSP00000261584.4:p.Pro4=
ENST00000567003.1:n.155C=
ENST00000568219.5:c.-858C=	ENSP00000454703.2:n.-858C=
NM_024675.3:c.11C= , LRG_308t1:c.11C=	NP_078951.2:p.Pro4=
XM_011545948.1:c.-1009C=	XP_011544250.1:n.-1009C=
XM_011545946.2:c.-842C=	XP_011544248.1:n.-842C=
XM_011545947.2:c.-842C=	XP_011544249.1:n.-842C=
XM_011545948.2:c.-1009C=	XP_011544250.1:n.-1009C=
XM_017023671.1:c.-842C=	XP_016879160.1:n.-842C=
XM_017023672.2:c.11C=	XP_016879161.1:p.Pro4=
XM_017023673.2:c.11C=	XP_016879162.1:p.Pro4=
NM_024675.4:c.11C= MANE Select	NP_078951.2:p.Pro4=