Canonical Allele Identifier: CA395137656

Gene: PALB2

Linked Data

• dbSNP Id: rs1966394739
• MyVariant Identifiers: chr16:g.23614793T>C (hg19) ; chr16:g.23603472T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603472T>C , CM000678.2:g.23603472T>C	GRCh38
NC_000016.9:g.23614793T>C , CM000678.1:g.23614793T>C	GRCh37
NC_000016.8:g.23522294T>C	NCBI36
NG_007406.1:g.42886A>G , LRG_308:g.42886A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3554A>G	ENSP00000460666.3:p.Tyr1185Cys
ENST00000565038.2:c.*1033A>G	ENSP00000459882.2:n.*1033A>G
ENST00000566069.6:c.*183A>G	ENSP00000459237.2:n.*183A>G
ENST00000697377.2:c.3392A>G	ENSP00000513286.2:p.Tyr1131Cys
ENST00000697379.2:c.3554A>G	ENSP00000513287.2:p.Tyr1185Cys
ENST00000561514.2:c.2663A>G	ENSP00000460666.2:p.Tyr888Cys
ENST00000697374.1:c.2663A>G	ENSP00000513284.1:p.Tyr888Cys
ENST00000697375.1:n.4895A>G
ENST00000697376.1:c.*183A>G	ENSP00000513285.1:n.*183A>G
ENST00000697377.1:c.2501A>G	ENSP00000513286.1:p.Tyr834Cys
ENST00000697378.1:n.4068A>G
ENST00000697379.1:c.2663A>G	ENSP00000513287.1:p.Tyr888Cys
ENST00000697380.1:n.2752A>G
ENST00000697381.1:n.2243A>G
ENST00000697382.1:c.*325A>G	ENSP00000513288.1:n.*325A>G
ENST00000697383.1:c.1082A>G	ENSP00000513289.1:p.Tyr361Cys
ENST00000261584.9:c.3548A>G MANE Select	ENSP00000261584.4:p.Tyr1183Cys
ENST00000261584.8:c.3548A>G	ENSP00000261584.4:p.Tyr1183Cys
ENST00000566069.5:c.314A>G
ENST00000568219.5:c.2663A>G	ENSP00000454703.2:p.Tyr888Cys
NM_024675.3:c.3548A>G , LRG_308t1:c.3548A>G	NP_078951.2:p.Tyr1183Cys
XM_011545946.1:c.3554A>G	XP_011544248.1:p.Tyr1185Cys
XM_011545947.1:c.*183A>G	XP_011544249.1:n.*183A>G
XM_011545948.1:c.2663A>G	XP_011544250.1:p.Tyr888Cys
XR_950851.1:n.4256A>G
XM_011545946.2:c.3554A>G	XP_011544248.1:p.Tyr1185Cys
XM_011545947.2:c.*183A>G	XP_011544249.1:n.*183A>G
XM_011545948.2:c.2663A>G	XP_011544250.1:p.Tyr888Cys
XM_017023671.1:c.3317A>G	XP_016879160.1:p.Tyr1106Cys
XM_017023672.2:c.3311A>G	XP_016879161.1:p.Tyr1104Cys
XM_017023673.2:c.*183A>G	XP_016879162.1:n.*183A>G
NM_024675.4:c.3548A>G MANE Select	NP_078951.2:p.Tyr1183Cys