Canonical Allele Identifier: CA395133449

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23646701A>T (hg19) ; chr16:g.23635380A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635380A>T , CM000678.2:g.23635380A>T	GRCh38
NC_000016.9:g.23646701A>T , CM000678.1:g.23646701A>T	GRCh37
NC_000016.8:g.23554202A>T	NCBI36
NG_007406.1:g.10978T>A , LRG_308:g.10978T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1172T>A	ENSP00000460666.3:p.Leu391His
ENST00000565038.2:c.211+2470T>A	ENSP00000459882.2:n.211+2470T>A
ENST00000566069.6:c.1166T>A	ENSP00000459237.2:p.Leu389His
ENST00000697377.2:c.1172T>A	ENSP00000513286.2:p.Leu391His
ENST00000697379.2:c.1172T>A	ENSP00000513287.2:p.Leu391His
ENST00000561514.2:c.281T>A	ENSP00000460666.2:p.Leu94His
ENST00000697374.1:c.281T>A	ENSP00000513284.1:p.Leu94His
ENST00000697375.1:n.2513T>A
ENST00000697376.1:c.281T>A	ENSP00000513285.1:p.Leu94His
ENST00000697377.1:c.281T>A	ENSP00000513286.1:p.Leu94His
ENST00000697378.1:n.1686T>A
ENST00000697379.1:c.281T>A	ENSP00000513287.1:p.Leu94His
ENST00000697382.1:c.281T>A	ENSP00000513288.1:p.Leu94His
ENST00000697383.1:c.48+5730T>A	ENSP00000513289.1:n.48+5730T>A
ENST00000697384.1:n.1320T>A
ENST00000261584.9:c.1166T>A MANE Select	ENSP00000261584.4:p.Leu389His
ENST00000261584.8:c.1166T>A	ENSP00000261584.4:p.Leu389His
ENST00000565038.1:c.86+2470T>A
ENST00000568219.5:c.281T>A	ENSP00000454703.2:p.Leu94His
NM_024675.3:c.1166T>A , LRG_308t1:c.1166T>A	NP_078951.2:p.Leu389His
XM_011545946.1:c.1172T>A	XP_011544248.1:p.Leu391His
XM_011545947.1:c.1172T>A	XP_011544249.1:p.Leu391His
XM_011545948.1:c.281T>A	XP_011544250.1:p.Leu94His
XR_950851.1:n.1962T>A
XM_011545946.2:c.1172T>A	XP_011544248.1:p.Leu391His
XM_011545947.2:c.1172T>A	XP_011544249.1:p.Leu391His
XM_011545948.2:c.281T>A	XP_011544250.1:p.Leu94His
XM_017023671.1:c.1172T>A	XP_016879160.1:p.Leu391His
XM_017023672.2:c.1166T>A	XP_016879161.1:p.Leu389His
XM_017023673.2:c.1166T>A	XP_016879162.1:p.Leu389His
NM_024675.4:c.1166T>A MANE Select	NP_078951.2:p.Leu389His