Canonical Allele Identifier: CA459678482

Gene: LPL

Linked Data

• MyVariant Identifiers: chr8:g.19809342A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.19951831A>C , CM000670.2:g.19951831A>C	GRCh38
NC_000008.10:g.19809342A>C , CM000670.1:g.19809342A>C	GRCh37
NC_000008.9:g.19853622A>C	NCBI36
NG_008855.1:g.17761A>C
NG_008855.2:g.55115A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650287.1:c.312A>C MANE Select	ENSP00000497642.1:p.Pro104=
ENST00000311322.8:c.312A>C	ENSP00000309757.6:p.Pro104=
ENST00000520959.5:c.84A>C	ENSP00000428496.1:p.Pro28=
ENST00000522701.5:c.312A>C	ENSP00000428557.1:p.Pro104=
ENST00000524029.5:c.312A>C	ENSP00000428237.1:p.Pro104=
NM_000237.2:c.312A>C	NP_000228.1:p.Pro104=
NM_000237.3:c.312A>C MANE Select	NP_000228.1:p.Pro104=