Canonical Allele Identifier: CA366351968

Gene: LPA

Linked Data

• MyVariant Identifiers: chr6:g.160969574T>A (hg19) ; chr6:g.160548542T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548542T>A , CM000668.2:g.160548542T>A	GRCh38
NC_000006.11:g.160969574T>A , CM000668.1:g.160969574T>A	GRCh37
NC_000006.10:g.160889564T>A	NCBI36
NG_016147.1:g.122834A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.5091A>T MANE Select	ENSP00000321334.6:p.Glu1697Asp
ENST00000316300.9:c.5091A>T	ENSP00000321334.5:p.Glu1697Asp
NM_005577.2:c.5091A>T	NP_005568.2:p.Glu1697Asp
NM_005577.3:c.5091A>T	NP_005568.2:p.Glu1697Asp
NM_005577.4:c.5091A>T MANE Select	NP_005568.2:p.Glu1697Asp