Canonical Allele Identifier: CA366352278

Gene: LPA

Linked Data

• MyVariant Identifiers: chr6:g.160969641C>A (hg19) ; chr6:g.160548609C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548609C>A , CM000668.2:g.160548609C>A	GRCh38
NC_000006.11:g.160969641C>A , CM000668.1:g.160969641C>A	GRCh37
NC_000006.10:g.160889631C>A	NCBI36
NG_016147.1:g.122767G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5024G>T MANE Select	ENSP00000321334.6:p.Trp1675Leu
ENST00000316300.9:c.5024G>T	ENSP00000321334.5:p.Trp1675Leu
NM_005577.2:c.5024G>T	NP_005568.2:p.Trp1675Leu
NM_005577.3:c.5024G>T	NP_005568.2:p.Trp1675Leu
NM_005577.4:c.5024G>T MANE Select	NP_005568.2:p.Trp1675Leu