Canonical Allele Identifier: CA2580575205
Gene: LPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541471T>G , CM000668.2:g.160541471T>G GRCh38
NC_000006.11:g.160962503T>G , CM000668.1:g.160962503T>G GRCh37
NC_000006.10:g.160882493T>G NCBI36
NG_016147.1:g.129905A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-290A>C MANE Select ENSP00000321334.6:n.5520-290A>C
ENST00000316300.9:c.5520-290A>C ENSP00000321334.5:n.5520-290A>C
NM_005577.2:c.5520-290A>C NP_005568.2:n.5520-290A>C
NM_005577.3:c.5520-290A>C NP_005568.2:n.5520-290A>C
NM_005577.4:c.5520-290A>C MANE Select NP_005568.2:n.5520-290A>C