Canonical Allele Identifier: CA395145032

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23635374A>T (hg19) ; chr16:g.23624053A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624053A>T , CM000678.2:g.23624053A>T	GRCh38
NC_000016.9:g.23635374A>T , CM000678.1:g.23635374A>T	GRCh37
NC_000016.8:g.23542875A>T	NCBI36
NG_007406.1:g.22305T>A , LRG_308:g.22305T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2796T>A	ENSP00000460666.3:p.Asn932Lys
ENST00000565038.2:c.*271T>A	ENSP00000459882.2:n.*271T>A
ENST00000566069.6:c.2790T>A	ENSP00000459237.2:p.Asn930Lys
ENST00000697377.2:c.2634T>A	ENSP00000513286.2:p.Asn878Lys
ENST00000697379.2:c.2796T>A	ENSP00000513287.2:p.Asn932Lys
ENST00000561514.2:c.1905T>A	ENSP00000460666.2:p.Asn635Lys
ENST00000697374.1:c.1905T>A	ENSP00000513284.1:p.Asn635Lys
ENST00000697375.1:n.4137T>A
ENST00000697376.1:c.1905T>A	ENSP00000513285.1:p.Asn635Lys
ENST00000697377.1:c.1743T>A	ENSP00000513286.1:p.Asn581Lys
ENST00000697378.1:n.3310T>A
ENST00000697379.1:c.1905T>A	ENSP00000513287.1:p.Asn635Lys
ENST00000697380.1:n.2082T>A
ENST00000697381.1:n.1485T>A
ENST00000697382.1:c.1905T>A	ENSP00000513288.1:p.Asn635Lys
ENST00000697383.1:c.324T>A	ENSP00000513289.1:p.Asn108Lys
ENST00000261584.9:c.2790T>A MANE Select	ENSP00000261584.4:p.Asn930Lys
ENST00000261584.8:c.2790T>A	ENSP00000261584.4:p.Asn930Lys
ENST00000568219.5:c.1905T>A	ENSP00000454703.2:p.Asn635Lys
NM_024675.3:c.2790T>A , LRG_308t1:c.2790T>A	NP_078951.2:p.Asn930Lys
XM_011545946.1:c.2796T>A	XP_011544248.1:p.Asn932Lys
XM_011545947.1:c.2796T>A	XP_011544249.1:p.Asn932Lys
XM_011545948.1:c.1905T>A	XP_011544250.1:p.Asn635Lys
XR_950851.1:n.3586T>A
XM_011545946.2:c.2796T>A	XP_011544248.1:p.Asn932Lys
XM_011545947.2:c.2796T>A	XP_011544249.1:p.Asn932Lys
XM_011545948.2:c.1905T>A	XP_011544250.1:p.Asn635Lys
XM_017023671.1:c.2796T>A	XP_016879160.1:p.Asn932Lys
XM_017023672.2:c.2790T>A	XP_016879161.1:p.Asn930Lys
XM_017023673.2:c.2790T>A	XP_016879162.1:p.Asn930Lys
NM_024675.4:c.2790T>A MANE Select	NP_078951.2:p.Asn930Lys