Canonical Allele Identifier: CA395137695

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23647519T>A (hg19) ; chr16:g.23636198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636198T>A , CM000678.2:g.23636198T>A	GRCh38
NC_000016.9:g.23647519T>A , CM000678.1:g.23647519T>A	GRCh37
NC_000016.8:g.23555020T>A	NCBI36
NG_007406.1:g.10160A>T , LRG_308:g.10160A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.354A>T	ENSP00000460666.3:p.Leu118Phe
ENST00000565038.2:c.211+1652A>T	ENSP00000459882.2:n.211+1652A>T
ENST00000566069.6:c.348A>T	ENSP00000459237.2:p.Leu116Phe
ENST00000697377.2:c.354A>T	ENSP00000513286.2:p.Leu118Phe
ENST00000697379.2:c.354A>T	ENSP00000513287.2:p.Leu118Phe
ENST00000561514.2:c.-538A>T	ENSP00000460666.2:n.-538A>T
ENST00000697374.1:c.-538A>T	ENSP00000513284.1:n.-538A>T
ENST00000697375.1:n.1695A>T
ENST00000697376.1:c.-538A>T	ENSP00000513285.1:n.-538A>T
ENST00000697377.1:c.-538A>T	ENSP00000513286.1:n.-538A>T
ENST00000697378.1:n.868A>T
ENST00000697379.1:c.-538A>T	ENSP00000513287.1:n.-538A>T
ENST00000697382.1:c.-538A>T	ENSP00000513288.1:n.-538A>T
ENST00000697383.1:c.48+4912A>T	ENSP00000513289.1:n.48+4912A>T
ENST00000697384.1:n.502A>T
ENST00000261584.9:c.348A>T MANE Select	ENSP00000261584.4:p.Leu116Phe
ENST00000261584.8:c.348A>T	ENSP00000261584.4:p.Leu116Phe
ENST00000565038.1:c.86+1652A>T
ENST00000567003.1:n.626A>T
ENST00000568219.5:c.-538A>T	ENSP00000454703.2:n.-538A>T
NM_024675.3:c.348A>T , LRG_308t1:c.348A>T	NP_078951.2:p.Leu116Phe
XM_011545946.1:c.354A>T	XP_011544248.1:p.Leu118Phe
XM_011545947.1:c.354A>T	XP_011544249.1:p.Leu118Phe
XM_011545948.1:c.-538A>T	XP_011544250.1:n.-538A>T
XR_950851.1:n.1144A>T
XM_011545946.2:c.354A>T	XP_011544248.1:p.Leu118Phe
XM_011545947.2:c.354A>T	XP_011544249.1:p.Leu118Phe
XM_011545948.2:c.-538A>T	XP_011544250.1:n.-538A>T
XM_017023671.1:c.354A>T	XP_016879160.1:p.Leu118Phe
XM_017023672.2:c.348A>T	XP_016879161.1:p.Leu116Phe
XM_017023673.2:c.348A>T	XP_016879162.1:p.Leu116Phe
NM_024675.4:c.348A>T MANE Select	NP_078951.2:p.Leu116Phe