Canonical Allele Identifier: CA2213436457

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641155C= , CM000678.2:g.23641155C=	GRCh38
NC_000016.9:g.23652476C= , CM000678.1:g.23652476C=	GRCh37
NC_000016.8:g.23559977C=	NCBI36
NG_007406.1:g.5203G= , LRG_308:g.5203G=

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.4:c.3G= MANE Select	NP_078951.2:p.Met1=
ENST00000261584.9:c.3G= MANE Select	ENSP00000261584.4:p.Met1=
NM_024675.3:c.3G= , LRG_308t1:c.3G=	NP_078951.2:p.Met1=
ENST00000261584.8:c.3G=	ENSP00000261584.4:p.Met1=
ENST00000561514.2:c.-1741G=	ENSP00000460666.2:n.-1741G=
ENST00000561514.3:c.-850G=	ENSP00000460666.3:n.-850G=
ENST00000565038.2:c.3G=	ENSP00000459882.2:p.Met1=
ENST00000566069.6:c.3G=	ENSP00000459237.2:p.Met1=
ENST00000567003.1:n.147G=
ENST00000568219.5:c.-866G=	ENSP00000454703.2:n.-866G=
ENST00000697374.1:c.-1332G=	ENSP00000513284.1:n.-1332G=
ENST00000697376.1:c.-1053G=	ENSP00000513285.1:n.-1053G=
ENST00000697377.1:c.-1128G=	ENSP00000513286.1:n.-1128G=
ENST00000697377.2:c.-237G=	ENSP00000513286.2:n.-237G=
ENST00000697379.1:c.-1034G=	ENSP00000513287.1:n.-1034G=
ENST00000697379.2:c.-143G=	ENSP00000513287.2:n.-143G=
ENST00000697382.1:c.-1792G=	ENSP00000513288.1:n.-1792G=
ENST00000697383.1:c.3G=	ENSP00000513289.1:p.Met1=
ENST00000697384.1:n.157G=
XM_011545946.2:c.-850G=	XP_011544248.1:n.-850G=
XM_011545947.2:c.-850G=	XP_011544249.1:n.-850G=
XM_011545948.1:c.-1017G=	XP_011544250.1:n.-1017G=
XM_011545948.2:c.-1017G=	XP_011544250.1:n.-1017G=
XM_017023671.1:c.-850G=	XP_016879160.1:n.-850G=
XM_017023672.2:c.3G=	XP_016879161.1:p.Met1=
XM_017023673.2:c.3G=	XP_016879162.1:p.Met1=