Canonical Allele Identifier: CA2213424433

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603573G= , CM000678.2:g.23603573G=	GRCh38
NC_000016.9:g.23614894G= , CM000678.1:g.23614894G=	GRCh37
NC_000016.8:g.23522395G=	NCBI36
NG_007406.1:g.42785C= , LRG_308:g.42785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3453C=	ENSP00000460666.3:p.Ala1151=
ENST00000565038.2:c.*932C=	ENSP00000459882.2:n.*932C=
ENST00000566069.6:c.*82C=	ENSP00000459237.2:n.*82C=
ENST00000697377.2:c.3291C=	ENSP00000513286.2:p.Ala1097=
ENST00000697379.2:c.3453C=	ENSP00000513287.2:p.Ala1151=
ENST00000561514.2:c.2562C=	ENSP00000460666.2:p.Ala854=
ENST00000697374.1:c.2562C=	ENSP00000513284.1:p.Ala854=
ENST00000697375.1:n.4794C=
ENST00000697376.1:c.*82C=	ENSP00000513285.1:n.*82C=
ENST00000697377.1:c.2400C=	ENSP00000513286.1:p.Ala800=
ENST00000697378.1:n.3967C=
ENST00000697379.1:c.2562C=	ENSP00000513287.1:p.Ala854=
ENST00000697380.1:n.2651C=
ENST00000697381.1:n.2142C=
ENST00000697382.1:c.*224C=	ENSP00000513288.1:n.*224C=
ENST00000697383.1:c.981C=	ENSP00000513289.1:p.Ala327=
ENST00000261584.9:c.3447C= MANE Select	ENSP00000261584.4:p.Ala1149=
ENST00000261584.8:c.3447C=	ENSP00000261584.4:p.Ala1149=
ENST00000566069.5:c.213C=
ENST00000568219.5:c.2562C=	ENSP00000454703.2:p.Ala854=
NM_024675.3:c.3447C= , LRG_308t1:c.3447C=	NP_078951.2:p.Ala1149=
XM_011545946.1:c.3453C=	XP_011544248.1:p.Ala1151=
XM_011545947.1:c.*82C=	XP_011544249.1:n.*82C=
XM_011545948.1:c.2562C=	XP_011544250.1:p.Ala854=
XR_950851.1:n.4155C=
XM_011545946.2:c.3453C=	XP_011544248.1:p.Ala1151=
XM_011545947.2:c.*82C=	XP_011544249.1:n.*82C=
XM_011545948.2:c.2562C=	XP_011544250.1:p.Ala854=
XM_017023671.1:c.3216C=	XP_016879160.1:p.Ala1072=
XM_017023672.2:c.3210C=	XP_016879161.1:p.Ala1070=
XM_017023673.2:c.*82C=	XP_016879162.1:n.*82C=
NM_024675.4:c.3447C= MANE Select	NP_078951.2:p.Ala1149=