Canonical Allele Identifier: CA645542101
Gene: PLG HGNC NCBI

Linked Data

COSMIC: COSM5016168
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160741326dup , CM000668.2:g.160741326dup GRCh38
NC_000006.11:g.161162358dup , CM000668.1:g.161162358dup GRCh37
NC_000006.10:g.161082348dup NCBI36
NG_016200.1:g.44134dup , LRG_571:g.44134dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.987dup ENSP00000516619.1:p.Asp330Ter
ENST00000418964.2:c.2085dup ENSP00000389424.2:p.Asp696Ter
ENST00000706906.1:c.*2054dup ENSP00000516618.1:n.*2054dup
ENST00000308192.14:c.2034dup MANE Select ENSP00000308938.9:p.Asp679Ter
ENST00000308192.13:c.2034dup ENSP00000308938.9:p.Asp679Ter
ENST00000461414.2:n.57dup
ENST00000467466.1:n.335dup
NM_000301.3:c.2034dup , LRG_571t1:c.2034dup NP_000292.1:p.Asp679Ter
NM_000301.4:c.2034dup NP_000292.1:p.Asp679Ter
NM_000301.5:c.2034dup MANE Select NP_000292.1:p.Asp679Ter
Search 100 bp 5'
Search 100 bp 3'