Canonical Allele Identifier: CA2681092792
Gene: PLG HGNC NCBI

Linked Data

gnomAD v4: 6-160741427-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160741427A>G , CM000668.2:g.160741427A>G GRCh38
NC_000006.11:g.161162459A>G , CM000668.1:g.161162459A>G GRCh37
NC_000006.10:g.161082449A>G NCBI36
NG_016200.1:g.44235A>G , LRG_571:g.44235A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297289.9:c.1078+10A>G ENSP00000516619.1:n.1078+10A>G
ENST00000418964.2:c.2176+10A>G ENSP00000389424.2:n.2176+10A>G
ENST00000706906.1:c.*2145+10A>G ENSP00000516618.1:n.*2145+10A>G
ENST00000308192.14:c.2125+10A>G MANE Select ENSP00000308938.9:n.2125+10A>G
ENST00000308192.13:c.2125+10A>G ENSP00000308938.9:n.2125+10A>G
ENST00000461414.2:n.99+59A>G
ENST00000467466.1:n.426+10A>G
NM_000301.3:c.2125+10A>G , LRG_571t1:c.2125+10A>G NP_000292.1:n.2125+10A>G
NM_000301.4:c.2125+10A>G NP_000292.1:n.2125+10A>G
NM_000301.5:c.2125+10A>G MANE Select NP_000292.1:n.2125+10A>G
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