Canonical Allele Identifier: CA370468605
Gene: LPL HGNC NCBI

Linked Data

gnomAD v4: 8-19954290-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954290A>T , CM000670.2:g.19954290A>T GRCh38
NC_000008.10:g.19811801A>T , CM000670.1:g.19811801A>T GRCh37
NC_000008.9:g.19856081A>T NCBI36
NG_008855.1:g.20220A>T
NG_008855.2:g.57574A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.712A>T MANE Select ENSP00000497642.1:p.Thr238Ser
ENST00000311322.8:c.712A>T ENSP00000309757.6:p.Thr238Ser
NM_000237.2:c.712A>T NP_000228.1:p.Thr238Ser
NM_000237.3:c.712A>T MANE Select NP_000228.1:p.Thr238Ser