Canonical Allele Identifier: CA151230165
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs568670520

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553603T>G , CM000668.2:g.160553603T>G GRCh38
NC_000006.11:g.160974635T>G , CM000668.1:g.160974635T>G GRCh37
NC_000006.10:g.160894625T>G NCBI36
NG_016147.1:g.117773A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2422A>C MANE Select ENSP00000321334.6:n.4973+2422A>C
ENST00000316300.9:c.4973+2422A>C ENSP00000321334.5:n.4973+2422A>C
NM_005577.2:c.4973+2422A>C NP_005568.2:n.4973+2422A>C
NM_005577.3:c.4973+2422A>C NP_005568.2:n.4973+2422A>C
NM_005577.4:c.4973+2422A>C MANE Select NP_005568.2:n.4973+2422A>C