Canonical Allele Identifier: CA395141106

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23625328T>A (hg19) ; chr16:g.23614007T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614007T>A , CM000678.2:g.23614007T>A	GRCh38
NC_000016.9:g.23625328T>A , CM000678.1:g.23625328T>A	GRCh37
NC_000016.8:g.23532829T>A	NCBI36
NG_007406.1:g.32351A>T , LRG_308:g.32351A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3204A>T	ENSP00000460666.3:p.Glu1068Asp
ENST00000565038.2:c.*679A>T	ENSP00000459882.2:n.*679A>T
ENST00000566069.6:c.3198A>T	ENSP00000459237.2:p.Glu1066Asp
ENST00000697377.2:c.3042A>T	ENSP00000513286.2:p.Glu1014Asp
ENST00000697379.2:c.3204A>T	ENSP00000513287.2:p.Glu1068Asp
ENST00000561514.2:c.2313A>T	ENSP00000460666.2:p.Glu771Asp
ENST00000697374.1:c.2313A>T	ENSP00000513284.1:p.Glu771Asp
ENST00000697375.1:n.4545A>T
ENST00000697376.1:c.2313A>T	ENSP00000513285.1:p.Glu771Asp
ENST00000697377.1:c.2151A>T	ENSP00000513286.1:p.Glu717Asp
ENST00000697378.1:n.3718A>T
ENST00000697379.1:c.2313A>T	ENSP00000513287.1:p.Glu771Asp
ENST00000697380.1:n.2406-5995A>T
ENST00000697381.1:n.1893A>T
ENST00000697382.1:c.2229-5995A>T	ENSP00000513288.1:n.2229-5995A>T
ENST00000697383.1:c.732A>T	ENSP00000513289.1:p.Glu244Asp
ENST00000261584.9:c.3198A>T MANE Select	ENSP00000261584.4:p.Glu1066Asp
ENST00000261584.8:c.3198A>T	ENSP00000261584.4:p.Glu1066Asp
ENST00000566069.5:c.113A>T
ENST00000568219.5:c.2313A>T	ENSP00000454703.2:p.Glu771Asp
NM_024675.3:c.3198A>T , LRG_308t1:c.3198A>T	NP_078951.2:p.Glu1066Asp
XM_011545946.1:c.3204A>T	XP_011544248.1:p.Glu1068Asp
XM_011545947.1:c.3204A>T	XP_011544249.1:p.Glu1068Asp
XM_011545948.1:c.2313A>T	XP_011544250.1:p.Glu771Asp
XR_950851.1:n.3910-5995A>T
XM_011545946.2:c.3204A>T	XP_011544248.1:p.Glu1068Asp
XM_011545947.2:c.3204A>T	XP_011544249.1:p.Glu1068Asp
XM_011545948.2:c.2313A>T	XP_011544250.1:p.Glu771Asp
XM_017023671.1:c.3119+7355A>T	XP_016879160.1:n.3119+7355A>T
XM_017023672.2:c.3113+7355A>T	XP_016879161.1:n.3113+7355A>T
XM_017023673.2:c.3198A>T	XP_016879162.1:p.Glu1066Asp
NM_024675.4:c.3198A>T MANE Select	NP_078951.2:p.Glu1066Asp