Canonical Allele Identifier: CA2528111732
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553511_160553514del , CM000668.2:g.160553511_160553514del GRCh38
NC_000006.11:g.160974543_160974546del , CM000668.1:g.160974543_160974546del GRCh37
NC_000006.10:g.160894533_160894536del NCBI36
NG_016147.1:g.117865_117868del

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2514_4973+2517del MANE Select ENSP00000321334.6:n.4973+2514_4973+2517del
ENST00000316300.9:c.4973+2514_4973+2517del ENSP00000321334.5:n.4973+2514_4973+2517del
NM_005577.2:c.4973+2514_4973+2517del NP_005568.2:n.4973+2514_4973+2517del
NM_005577.3:c.4973+2514_4973+2517del NP_005568.2:n.4973+2514_4973+2517del
NM_005577.4:c.4973+2514_4973+2517del MANE Select NP_005568.2:n.4973+2514_4973+2517del
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