Canonical Allele Identifier: CA2605766348

Gene: LPA

Linked Data

• dbSNP Id: rs2115008178
• gnomAD v3: 6-160553495-A-G
• gnomAD v4: 6-160553495-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160553495A>G , CM000668.2:g.160553495A>G	GRCh38
NC_000006.11:g.160974527A>G , CM000668.1:g.160974527A>G	GRCh37
NC_000006.10:g.160894517A>G	NCBI36
NG_016147.1:g.117881T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4973+2530T>C MANE Select	ENSP00000321334.6:n.4973+2530T>C
ENST00000316300.9:c.4973+2530T>C	ENSP00000321334.5:n.4973+2530T>C
NM_005577.2:c.4973+2530T>C	NP_005568.2:n.4973+2530T>C
NM_005577.3:c.4973+2530T>C	NP_005568.2:n.4973+2530T>C
NM_005577.4:c.4973+2530T>C MANE Select	NP_005568.2:n.4973+2530T>C