Canonical Allele Identifier: CA370468536
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954255C>T , CM000670.2:g.19954255C>T GRCh38
NC_000008.10:g.19811766C>T , CM000670.1:g.19811766C>T GRCh37
NC_000008.9:g.19856046C>T NCBI36
NG_008855.1:g.20185C>T
NG_008855.2:g.57539C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.677C>T MANE Select ENSP00000497642.1:p.Pro226Leu
ENST00000311322.8:c.677C>T ENSP00000309757.6:p.Pro226Leu
NM_000237.2:c.677C>T NP_000228.1:p.Pro226Leu
NM_000237.3:c.677C>T MANE Select NP_000228.1:p.Pro226Leu