Canonical Allele Identifier: CA459879523
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811812A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954301A>T , CM000670.2:g.19954301A>T GRCh38
NC_000008.10:g.19811812A>T , CM000670.1:g.19811812A>T GRCh37
NC_000008.9:g.19856092A>T NCBI36
NG_008855.1:g.20231A>T
NG_008855.2:g.57585A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.723A>T MANE Select ENSP00000497642.1:p.Pro241=
ENST00000311322.8:c.723A>T ENSP00000309757.6:p.Pro241=
NM_000237.2:c.723A>T NP_000228.1:p.Pro241=
NM_000237.3:c.723A>T MANE Select NP_000228.1:p.Pro241=