Canonical Allele Identifier: CA370467729
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951925G>T , CM000670.2:g.19951925G>T GRCh38
NC_000008.10:g.19809436G>T , CM000670.1:g.19809436G>T GRCh37
NC_000008.9:g.19853716G>T NCBI36
NG_008855.1:g.17855G>T
NG_008855.2:g.55209G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.406G>T MANE Select ENSP00000497642.1:p.Ala136Ser
ENST00000311322.8:c.406G>T ENSP00000309757.6:p.Ala136Ser
ENST00000520959.5:c.178G>T ENSP00000428496.1:p.Ala60Ser
NM_000237.2:c.406G>T NP_000228.1:p.Ala136Ser
NM_000237.3:c.406G>T MANE Select NP_000228.1:p.Ala136Ser