Canonical Allele Identifier: CA459879299
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811641A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954130A>T , CM000670.2:g.19954130A>T GRCh38
NC_000008.10:g.19811641A>T , CM000670.1:g.19811641A>T GRCh37
NC_000008.9:g.19855921A>T NCBI36
NG_008855.1:g.20060A>T
NG_008855.2:g.57414A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.552A>T MANE Select ENSP00000497642.1:p.Pro184=
ENST00000311322.8:c.552A>T ENSP00000309757.6:p.Pro184=
ENST00000520959.5:c.324A>T ENSP00000428496.1:p.Pro108=
NM_000237.2:c.552A>T NP_000228.1:p.Pro184=
NM_000237.3:c.552A>T MANE Select NP_000228.1:p.Pro184=