Canonical Allele Identifier: CA1769110518

Gene: LPL

Linked Data

• dbSNP Id: rs2070031363

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19960801T>C , CM000670.2:g.19960801T>C	GRCh38
NC_000008.10:g.19818312T>C , CM000670.1:g.19818312T>C	GRCh37
NC_000008.9:g.19862592T>C	NCBI36
NG_008855.1:g.26731T>C
NG_008855.2:g.64085T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650287.1:c.1140-100T>C MANE Select	ENSP00000497642.1:n.1140-100T>C
ENST00000650478.1:c.80-100T>C	ENSP00000497560.1:n.80-100T>C
ENST00000311322.8:c.1140-100T>C	ENSP00000309757.6:n.1140-100T>C
NM_000237.2:c.1140-100T>C	NP_000228.1:n.1140-100T>C
NM_000237.3:c.1140-100T>C MANE Select	NP_000228.1:n.1140-100T>C