Canonical Allele Identifier: CA1096555555
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1778198224
gnomAD v3: 6-160553474-T-G
gnomAD v4: 6-160553474-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553474T>G , CM000668.2:g.160553474T>G GRCh38
NC_000006.11:g.160974506T>G , CM000668.1:g.160974506T>G GRCh37
NC_000006.10:g.160894496T>G NCBI36
NG_016147.1:g.117902A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2551A>C MANE Select ENSP00000321334.6:n.4973+2551A>C
ENST00000316300.9:c.4973+2551A>C ENSP00000321334.5:n.4973+2551A>C
NM_005577.2:c.4973+2551A>C NP_005568.2:n.4973+2551A>C
NM_005577.3:c.4973+2551A>C NP_005568.2:n.4973+2551A>C
NM_005577.4:c.4973+2551A>C MANE Select NP_005568.2:n.4973+2551A>C
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