Canonical Allele Identifier: CA1096550688
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1777983039
gnomAD v3: 6-160541614-A-T
gnomAD v4: 6-160541614-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541614A>T , CM000668.2:g.160541614A>T GRCh38
NC_000006.11:g.160962646A>T , CM000668.1:g.160962646A>T GRCh37
NC_000006.10:g.160882636A>T NCBI36
NG_016147.1:g.129762T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.5520-433T>A MANE Select ENSP00000321334.6:n.5520-433T>A
ENST00000316300.9:c.5520-433T>A ENSP00000321334.5:n.5520-433T>A
NM_005577.2:c.5520-433T>A NP_005568.2:n.5520-433T>A
NM_005577.3:c.5520-433T>A NP_005568.2:n.5520-433T>A
NM_005577.4:c.5520-433T>A MANE Select NP_005568.2:n.5520-433T>A
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