Canonical Allele Identifier: CA151230125

Gene: LPA

Linked Data

• dbSNP Id: rs1039505384
• MyVariant Identifiers: chr6:g.160974616C>T (hg19) ; chr6:g.160553584C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553584C>T , CM000668.2:g.160553584C>T	GRCh38
NC_000006.11:g.160974616C>T , CM000668.1:g.160974616C>T	GRCh37
NC_000006.10:g.160894606C>T	NCBI36
NG_016147.1:g.117792G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4973+2441G>A MANE Select	ENSP00000321334.6:n.4973+2441G>A
ENST00000316300.9:c.4973+2441G>A	ENSP00000321334.5:n.4973+2441G>A
NM_005577.2:c.4973+2441G>A	NP_005568.2:n.4973+2441G>A
NM_005577.3:c.4973+2441G>A	NP_005568.2:n.4973+2441G>A
NM_005577.4:c.4973+2441G>A MANE Select	NP_005568.2:n.4973+2441G>A