Canonical Allele Identifier: CA453028927
Gene: PLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.161157926T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160736894T>C , CM000668.2:g.160736894T>C GRCh38
NC_000006.11:g.161157926T>C , CM000668.1:g.161157926T>C GRCh37
NC_000006.10:g.161077916T>C NCBI36
NG_016200.1:g.39702T>C , LRG_571:g.39702T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.642T>C ENSP00000516619.1:p.Pro214=
ENST00000418964.2:c.1740T>C ENSP00000389424.2:p.Pro580=
ENST00000706906.1:c.*1709T>C ENSP00000516618.1:n.*1709T>C
ENST00000308192.14:c.1689T>C MANE Select ENSP00000308938.9:p.Pro563=
ENST00000308192.13:c.1689T>C ENSP00000308938.9:p.Pro563=
NM_000301.3:c.1689T>C , LRG_571t1:c.1689T>C NP_000292.1:p.Pro563=
NM_000301.4:c.1689T>C NP_000292.1:p.Pro563=
NM_000301.5:c.1689T>C MANE Select NP_000292.1:p.Pro563=