Canonical Allele Identifier: CA1677112010
Gene: LPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160548720_160548721delinsAC , CM000668.2:g.160548720_160548721delinsAC GRCh38
NC_000006.11:g.160969752_160969753delinsAC , CM000668.1:g.160969752_160969753delinsAC GRCh37
NC_000006.10:g.160889742_160889743delinsAC NCBI36
NG_016147.1:g.122655_122656delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.4974-62_4974-61delinsGT MANE Select ENSP00000321334.6:n.4974-62_4974-61delins...
ENST00000316300.9:c.4974-62_4974-61delinsGT ENSP00000321334.5:n.4974-62_4974-61delins...
NM_005577.2:c.4974-62_4974-61delinsGT NP_005568.2:n.4974-62_4974-61delinsGT
NM_005577.3:c.4974-62_4974-61delinsGT NP_005568.2:n.4974-62_4974-61delinsGT
NM_005577.4:c.4974-62_4974-61delinsGT MANE Select NP_005568.2:n.4974-62_4974-61delinsGT
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