Canonical Allele Identifier: CA395143965

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23634317T>G (hg19) ; chr16:g.23622996T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23622996T>G , CM000678.2:g.23622996T>G	GRCh38
NC_000016.9:g.23634317T>G , CM000678.1:g.23634317T>G	GRCh37
NC_000016.8:g.23541818T>G	NCBI36
NG_007406.1:g.23362A>C , LRG_308:g.23362A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2975A>C	ENSP00000460666.3:p.Glu992Ala
ENST00000565038.2:c.*450A>C	ENSP00000459882.2:n.*450A>C
ENST00000566069.6:c.2969A>C	ENSP00000459237.2:p.Glu990Ala
ENST00000697377.2:c.2813A>C	ENSP00000513286.2:p.Glu938Ala
ENST00000697379.2:c.2975A>C	ENSP00000513287.2:p.Glu992Ala
ENST00000561514.2:c.2084A>C	ENSP00000460666.2:p.Glu695Ala
ENST00000697374.1:c.2084A>C	ENSP00000513284.1:p.Glu695Ala
ENST00000697375.1:n.4316A>C
ENST00000697376.1:c.2084A>C	ENSP00000513285.1:p.Glu695Ala
ENST00000697377.1:c.1922A>C	ENSP00000513286.1:p.Glu641Ala
ENST00000697378.1:n.3489A>C
ENST00000697379.1:c.2084A>C	ENSP00000513287.1:p.Glu695Ala
ENST00000697380.1:n.2261A>C
ENST00000697381.1:n.1664A>C
ENST00000697382.1:c.2084A>C	ENSP00000513288.1:p.Glu695Ala
ENST00000697383.1:c.503A>C	ENSP00000513289.1:p.Glu168Ala
ENST00000261584.9:c.2969A>C MANE Select	ENSP00000261584.4:p.Glu990Ala
ENST00000261584.8:c.2969A>C	ENSP00000261584.4:p.Glu990Ala
ENST00000568219.5:c.2084A>C	ENSP00000454703.2:p.Glu695Ala
NM_024675.3:c.2969A>C , LRG_308t1:c.2969A>C	NP_078951.2:p.Glu990Ala
XM_011545946.1:c.2975A>C	XP_011544248.1:p.Glu992Ala
XM_011545947.1:c.2975A>C	XP_011544249.1:p.Glu992Ala
XM_011545948.1:c.2084A>C	XP_011544250.1:p.Glu695Ala
XR_950851.1:n.3765A>C
XM_011545946.2:c.2975A>C	XP_011544248.1:p.Glu992Ala
XM_011545947.2:c.2975A>C	XP_011544249.1:p.Glu992Ala
XM_011545948.2:c.2084A>C	XP_011544250.1:p.Glu695Ala
XM_017023671.1:c.2975A>C	XP_016879160.1:p.Glu992Ala
XM_017023672.2:c.2969A>C	XP_016879161.1:p.Glu990Ala
XM_017023673.2:c.2969A>C	XP_016879162.1:p.Glu990Ala
NM_024675.4:c.2969A>C MANE Select	NP_078951.2:p.Glu990Ala