Canonical Allele Identifier: CA370467544
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19951836-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19951836C>T , CM000670.2:g.19951836C>T GRCh38
NC_000008.10:g.19809347C>T , CM000670.1:g.19809347C>T GRCh37
NC_000008.9:g.19853627C>T NCBI36
NG_008855.1:g.17766C>T
NG_008855.2:g.55120C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.317C>T MANE Select ENSP00000497642.1:p.Ser106Phe
ENST00000311322.8:c.317C>T ENSP00000309757.6:p.Ser106Phe
ENST00000520959.5:c.89C>T ENSP00000428496.1:p.Ser30Phe
ENST00000522701.5:c.317C>T
ENST00000524029.5:c.317C>T ENSP00000428237.1:p.Ser106Phe
NM_000237.2:c.317C>T NP_000228.1:p.Ser106Phe
NM_000237.3:c.317C>T MANE Select NP_000228.1:p.Ser106Phe