Canonical Allele Identifier: CA1677116136
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553497G= , CM000668.2:g.160553497G= GRCh38
NC_000006.11:g.160974529G= , CM000668.1:g.160974529G= GRCh37
NC_000006.10:g.160894519G= NCBI36
NG_016147.1:g.117879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2528C= MANE Select ENSP00000321334.6:n.4973+2528C=
ENST00000316300.9:c.4973+2528C= ENSP00000321334.5:n.4973+2528C=
NM_005577.2:c.4973+2528C= NP_005568.2:n.4973+2528C=
NM_005577.3:c.4973+2528C= NP_005568.2:n.4973+2528C=
NM_005577.4:c.4973+2528C= MANE Select NP_005568.2:n.4973+2528C=
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