Canonical Allele Identifier: CA651097111
Gene: LPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548706_160548707insG , CM000668.2:g.160548706_160548707insG GRCh38
NC_000006.11:g.160969738_160969739insG , CM000668.1:g.160969738_160969739insG GRCh37
NC_000006.10:g.160889728_160889729insG NCBI36
NG_016147.1:g.122669_122670insC

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-48_4974-47insC MANE Select ENSP00000321334.6:n.4974-48_4974-47insC
ENST00000316300.9:c.4974-48_4974-47insC ENSP00000321334.5:n.4974-48_4974-47insC
NM_005577.2:c.4974-48_4974-47insC NP_005568.2:n.4974-48_4974-47insC
NM_005577.3:c.4974-48_4974-47insC NP_005568.2:n.4974-48_4974-47insC
NM_005577.4:c.4974-48_4974-47insC MANE Select NP_005568.2:n.4974-48_4974-47insC