Canonical Allele Identifier: CA1677116122
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553486T= , CM000668.2:g.160553486T= GRCh38
NC_000006.11:g.160974518T= , CM000668.1:g.160974518T= GRCh37
NC_000006.10:g.160894508T= NCBI36
NG_016147.1:g.117890A=

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4973+2539A= MANE Select ENSP00000321334.6:n.4973+2539A=
ENST00000316300.9:c.4973+2539A= ENSP00000321334.5:n.4973+2539A=
NM_005577.2:c.4973+2539A= NP_005568.2:n.4973+2539A=
NM_005577.3:c.4973+2539A= NP_005568.2:n.4973+2539A=
NM_005577.4:c.4973+2539A= MANE Select NP_005568.2:n.4973+2539A=
Search 100 bp 5'
Search 100 bp 3'