Canonical Allele Identifier: CA370638621
Gene: LPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19960951T>G , CM000670.2:g.19960951T>G GRCh38
NC_000008.10:g.19818462T>G , CM000670.1:g.19818462T>G GRCh37
NC_000008.9:g.19862742T>G NCBI36
NG_008855.1:g.26881T>G
NG_008855.2:g.64235T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.1190T>G MANE Select ENSP00000497642.1:p.Val397Gly
ENST00000650478.1:c.130T>G ENSP00000497560.1:n.130T>G
ENST00000311322.8:c.1190T>G ENSP00000309757.6:p.Val397Gly
NM_000237.2:c.1190T>G NP_000228.1:p.Val397Gly
NM_000237.3:c.1190T>G MANE Select NP_000228.1:p.Val397Gly