Canonical Allele Identifier: CA1769101624
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1590143036

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954008G>C , CM000670.2:g.19954008G>C GRCh38
NC_000008.10:g.19811519G>C , CM000670.1:g.19811519G>C GRCh37
NC_000008.9:g.19855799G>C NCBI36
NG_008855.1:g.19938G>C
NG_008855.2:g.57292G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.542-112G>C MANE Select ENSP00000497642.1:n.542-112G>C
ENST00000311322.8:c.542-112G>C ENSP00000309757.6:n.542-112G>C
ENST00000520959.5:c.314-112G>C ENSP00000428496.1:n.314-112G>C
NM_000237.2:c.542-112G>C NP_000228.1:n.542-112G>C
NM_000237.3:c.542-112G>C MANE Select NP_000228.1:n.542-112G>C