Canonical Allele Identifier: CA1677107697
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs1777981257
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541487G>T , CM000668.2:g.160541487G>T GRCh38
NC_000006.11:g.160962519G>T , CM000668.1:g.160962519G>T GRCh37
NC_000006.10:g.160882509G>T NCBI36
NG_016147.1:g.129889C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-306C>A MANE Select ENSP00000321334.6:n.5520-306C>A
ENST00000316300.9:c.5520-306C>A ENSP00000321334.5:n.5520-306C>A
NM_005577.2:c.5520-306C>A NP_005568.2:n.5520-306C>A
NM_005577.3:c.5520-306C>A NP_005568.2:n.5520-306C>A
NM_005577.4:c.5520-306C>A MANE Select NP_005568.2:n.5520-306C>A
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