Canonical Allele Identifier: CA370468414
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954197G>T , CM000670.2:g.19954197G>T GRCh38
NC_000008.10:g.19811708G>T , CM000670.1:g.19811708G>T GRCh37
NC_000008.9:g.19855988G>T NCBI36
NG_008855.1:g.20127G>T
NG_008855.2:g.57481G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.619G>T MANE Select ENSP00000497642.1:p.Asp207Tyr
ENST00000311322.8:c.619G>T ENSP00000309757.6:p.Asp207Tyr
NM_000237.2:c.619G>T NP_000228.1:p.Asp207Tyr
NM_000237.3:c.619G>T MANE Select NP_000228.1:p.Asp207Tyr