Canonical Allele Identifier: CA1677116257
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1778200919

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553604G>A , CM000668.2:g.160553604G>A GRCh38
NC_000006.11:g.160974636G>A , CM000668.1:g.160974636G>A GRCh37
NC_000006.10:g.160894626G>A NCBI36
NG_016147.1:g.117772C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2421C>T MANE Select ENSP00000321334.6:n.4973+2421C>T
ENST00000316300.9:c.4973+2421C>T ENSP00000321334.5:n.4973+2421C>T
NM_005577.2:c.4973+2421C>T NP_005568.2:n.4973+2421C>T
NM_005577.3:c.4973+2421C>T NP_005568.2:n.4973+2421C>T
NM_005577.4:c.4973+2421C>T MANE Select NP_005568.2:n.4973+2421C>T