Canonical Allele Identifier: CA395144447

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23634427A>C (hg19) ; chr16:g.23623106A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623106A>C , CM000678.2:g.23623106A>C	GRCh38
NC_000016.9:g.23634427A>C , CM000678.1:g.23634427A>C	GRCh37
NC_000016.8:g.23541928A>C	NCBI36
NG_007406.1:g.23252T>G , LRG_308:g.23252T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2865T>G	ENSP00000460666.3:p.Asp955Glu
ENST00000565038.2:c.*340T>G	ENSP00000459882.2:n.*340T>G
ENST00000566069.6:c.2859T>G	ENSP00000459237.2:p.Asp953Glu
ENST00000697377.2:c.2703T>G	ENSP00000513286.2:p.Asp901Glu
ENST00000697379.2:c.2865T>G	ENSP00000513287.2:p.Asp955Glu
ENST00000561514.2:c.1974T>G	ENSP00000460666.2:p.Asp658Glu
ENST00000697374.1:c.1974T>G	ENSP00000513284.1:p.Asp658Glu
ENST00000697375.1:n.4206T>G
ENST00000697376.1:c.1974T>G	ENSP00000513285.1:p.Asp658Glu
ENST00000697377.1:c.1812T>G	ENSP00000513286.1:p.Asp604Glu
ENST00000697378.1:n.3379T>G
ENST00000697379.1:c.1974T>G	ENSP00000513287.1:p.Asp658Glu
ENST00000697380.1:n.2151T>G
ENST00000697381.1:n.1554T>G
ENST00000697382.1:c.1974T>G	ENSP00000513288.1:p.Asp658Glu
ENST00000697383.1:c.393T>G	ENSP00000513289.1:p.Asp131Glu
ENST00000261584.9:c.2859T>G MANE Select	ENSP00000261584.4:p.Asp953Glu
ENST00000261584.8:c.2859T>G	ENSP00000261584.4:p.Asp953Glu
ENST00000568219.5:c.1974T>G	ENSP00000454703.2:p.Asp658Glu
NM_024675.3:c.2859T>G , LRG_308t1:c.2859T>G	NP_078951.2:p.Asp953Glu
XM_011545946.1:c.2865T>G	XP_011544248.1:p.Asp955Glu
XM_011545947.1:c.2865T>G	XP_011544249.1:p.Asp955Glu
XM_011545948.1:c.1974T>G	XP_011544250.1:p.Asp658Glu
XR_950851.1:n.3655T>G
XM_011545946.2:c.2865T>G	XP_011544248.1:p.Asp955Glu
XM_011545947.2:c.2865T>G	XP_011544249.1:p.Asp955Glu
XM_011545948.2:c.1974T>G	XP_011544250.1:p.Asp658Glu
XM_017023671.1:c.2865T>G	XP_016879160.1:p.Asp955Glu
XM_017023672.2:c.2859T>G	XP_016879161.1:p.Asp953Glu
XM_017023673.2:c.2859T>G	XP_016879162.1:p.Asp953Glu
NM_024675.4:c.2859T>G MANE Select	NP_078951.2:p.Asp953Glu