Canonical Allele Identifier: CA123971
Gene: LPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160650438G>A , CM000668.2:g.160650438G>A GRCh38
NC_000006.11:g.161071470G>A , CM000668.1:g.161071470G>A GRCh37
NC_000006.10:g.160991460G>A NCBI36
NG_016147.1:g.20938C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.109C>T MANE Select ENSP00000321334.6:p.Arg37Ter
ENST00000316300.9:c.109C>T ENSP00000321334.5:p.Arg37Ter
NM_005577.2:c.109C>T NP_005568.2:p.Arg37Ter
NM_005577.3:c.109C>T NP_005568.2:p.Arg37Ter
NM_005577.4:c.109C>T MANE Select NP_005568.2:p.Arg37Ter