Canonical Allele Identifier: CA370468405
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954193T>A , CM000670.2:g.19954193T>A GRCh38
NC_000008.10:g.19811704T>A , CM000670.1:g.19811704T>A GRCh37
NC_000008.9:g.19855984T>A NCBI36
NG_008855.1:g.20123T>A
NG_008855.2:g.57477T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.615T>A MANE Select ENSP00000497642.1:p.Phe205Leu
ENST00000311322.8:c.615T>A ENSP00000309757.6:p.Phe205Leu
NM_000237.2:c.615T>A NP_000228.1:p.Phe205Leu
NM_000237.3:c.615T>A MANE Select NP_000228.1:p.Phe205Leu