Canonical Allele Identifier: CA1677201390
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160731210T= , CM000668.2:g.160731210T= GRCh38
NC_000006.11:g.161152242T= , CM000668.1:g.161152242T= GRCh37
NC_000006.10:g.161072232T= NCBI36
NG_016200.1:g.34018T= , LRG_571:g.34018T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.369T= ENSP00000516619.1:p.Asp123=
ENST00000418964.2:c.1467T= ENSP00000389424.2:p.Asp489=
ENST00000706906.1:c.1416T= ENSP00000516618.1:p.Asp472=
ENST00000308192.14:c.1416T= MANE Select ENSP00000308938.9:p.Asp472=
ENST00000297289.8:n.414T=
ENST00000308192.13:c.1416T= ENSP00000308938.9:p.Asp472=
ENST00000493435.1:n.471T=
NM_000301.3:c.1416T= , LRG_571t1:c.1416T= NP_000292.1:p.Asp472=
NM_000301.4:c.1416T= NP_000292.1:p.Asp472=
NM_000301.5:c.1416T= MANE Select NP_000292.1:p.Asp472=