Canonical Allele Identifier: CA1677116205
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553563A= , CM000668.2:g.160553563A= GRCh38
NC_000006.11:g.160974595A= , CM000668.1:g.160974595A= GRCh37
NC_000006.10:g.160894585A= NCBI36
NG_016147.1:g.117813T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2462T= MANE Select ENSP00000321334.6:n.4973+2462T=
ENST00000316300.9:c.4973+2462T= ENSP00000321334.5:n.4973+2462T=
NM_005577.2:c.4973+2462T= NP_005568.2:n.4973+2462T=
NM_005577.3:c.4973+2462T= NP_005568.2:n.4973+2462T=
NM_005577.4:c.4973+2462T= MANE Select NP_005568.2:n.4973+2462T=
Search 100 bp 5'
Search 100 bp 3'