Canonical Allele Identifier: CA1769104179
Gene: LPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19955550C= , CM000670.2:g.19955550C= GRCh38
NC_000008.10:g.19813061C= , CM000670.1:g.19813061C= GRCh37
NC_000008.9:g.19857341C= NCBI36
NG_008855.1:g.21480C=
NG_008855.2:g.58834C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.776-291C= MANE Select ENSP00000497642.1:n.776-291C=
ENST00000311322.8:c.776-291C= ENSP00000309757.6:n.776-291C=
NM_000237.2:c.776-291C= NP_000228.1:n.776-291C=
NM_000237.3:c.776-291C= MANE Select NP_000228.1:n.776-291C=