Canonical Allele Identifier: CA459879395
Gene: LPL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.19811689T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954178T>C , CM000670.2:g.19954178T>C GRCh38
NC_000008.10:g.19811689T>C , CM000670.1:g.19811689T>C GRCh37
NC_000008.9:g.19855969T>C NCBI36
NG_008855.1:g.20108T>C
NG_008855.2:g.57462T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.600T>C MANE Select ENSP00000497642.1:p.Pro200=
ENST00000311322.8:c.600T>C ENSP00000309757.6:p.Pro200=
NM_000237.2:c.600T>C NP_000228.1:p.Pro200=
NM_000237.3:c.600T>C MANE Select NP_000228.1:p.Pro200=