Canonical Allele Identifier: CA1677107690
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541480C= , CM000668.2:g.160541480C= GRCh38
NC_000006.11:g.160962512C= , CM000668.1:g.160962512C= GRCh37
NC_000006.10:g.160882502C= NCBI36
NG_016147.1:g.129896G=

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-299G= MANE Select ENSP00000321334.6:n.5520-299G=
ENST00000316300.9:c.5520-299G= ENSP00000321334.5:n.5520-299G=
NM_005577.2:c.5520-299G= NP_005568.2:n.5520-299G=
NM_005577.3:c.5520-299G= NP_005568.2:n.5520-299G=
NM_005577.4:c.5520-299G= MANE Select NP_005568.2:n.5520-299G=
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