Canonical Allele Identifier: CA366365176
Gene: PLG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160738593G>T , CM000668.2:g.160738593G>T GRCh38
NC_000006.11:g.161159625G>T , CM000668.1:g.161159625G>T GRCh37
NC_000006.10:g.161079615G>T NCBI36
NG_016200.1:g.41401G>T , LRG_571:g.41401G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297289.9:c.811G>T ENSP00000516619.1:p.Ala271Ser
ENST00000418964.2:c.1909G>T ENSP00000389424.2:p.Ala637Ser
ENST00000706906.1:c.*1878G>T ENSP00000516618.1:n.*1878G>T
ENST00000308192.14:c.1858G>T MANE Select ENSP00000308938.9:p.Ala620Ser
ENST00000308192.13:c.1858G>T ENSP00000308938.9:p.Ala620Ser
ENST00000467466.1:n.159G>T
NM_000301.3:c.1858G>T , LRG_571t1:c.1858G>T NP_000292.1:p.Ala620Ser
NM_000301.4:c.1858G>T NP_000292.1:p.Ala620Ser
NM_000301.5:c.1858G>T MANE Select NP_000292.1:p.Ala620Ser