Canonical Allele Identifier: CA2213428959

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23608005A= , CM000678.2:g.23608005A=	GRCh38
NC_000016.9:g.23619326A= , CM000678.1:g.23619326A=	GRCh37
NC_000016.8:g.23526827A=	NCBI36
NG_007406.1:g.38353T= , LRG_308:g.38353T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3215T=	ENSP00000460666.3:p.Leu1072=
ENST00000565038.2:c.*690T=	ENSP00000459882.2:n.*690T=
ENST00000566069.6:c.3202-4336T=	ENSP00000459237.2:n.3202-4336T=
ENST00000697377.2:c.3053T=	ENSP00000513286.2:p.Leu1018=
ENST00000697379.2:c.3215T=	ENSP00000513287.2:p.Leu1072=
ENST00000561514.2:c.2324T=	ENSP00000460666.2:p.Leu775=
ENST00000697374.1:c.2324T=	ENSP00000513284.1:p.Leu775=
ENST00000697375.1:n.4556T=
ENST00000697376.1:c.2317-4336T=	ENSP00000513285.1:n.2317-4336T=
ENST00000697377.1:c.2162T=	ENSP00000513286.1:p.Leu721=
ENST00000697378.1:n.3729T=
ENST00000697379.1:c.2324T=	ENSP00000513287.1:p.Leu775=
ENST00000697380.1:n.2413T=
ENST00000697381.1:n.1904T=
ENST00000697382.1:c.2236T=	ENSP00000513288.1:p.Ser746=
ENST00000697383.1:c.743T=	ENSP00000513289.1:p.Leu248=
ENST00000261584.9:c.3209T= MANE Select	ENSP00000261584.4:p.Leu1070=
ENST00000261584.8:c.3209T=	ENSP00000261584.4:p.Leu1070=
ENST00000566069.5:c.117-4336T=
ENST00000568219.5:c.2324T=	ENSP00000454703.2:p.Leu775=
NM_024675.3:c.3209T= , LRG_308t1:c.3209T=	NP_078951.2:p.Leu1070=
XM_011545946.1:c.3215T=	XP_011544248.1:p.Leu1072=
XM_011545947.1:c.3208-4336T=	XP_011544249.1:n.3208-4336T=
XM_011545948.1:c.2324T=	XP_011544250.1:p.Leu775=
XR_950851.1:n.3917T=
XM_011545946.2:c.3215T=	XP_011544248.1:p.Leu1072=
XM_011545947.2:c.3208-4336T=	XP_011544249.1:n.3208-4336T=
XM_011545948.2:c.2324T=	XP_011544250.1:p.Leu775=
XM_017023671.1:c.3120-4336T=	XP_016879160.1:n.3120-4336T=
XM_017023672.2:c.3114-4336T=	XP_016879161.1:n.3114-4336T=
XM_017023673.2:c.3202-4336T=	XP_016879162.1:n.3202-4336T=
NM_024675.4:c.3209T= MANE Select	NP_078951.2:p.Leu1070=