Canonical Allele Identifier: CA4086125

Gene: LPA

Linked Data

• ClinVar Variation Id: 403043
• ClinVar RCV Id: RCV000455185 ; RCV001823905
• dbSNP Id: rs41272114
• ExAC: 6:161006077 C / T
• gnomAD v2: 6-161006077-C-T
• gnomAD v3: 6-160585045-C-T
• gnomAD v4: 6-160585045-C-T
• MyVariant Identifiers: chr6:g.161006077C>T (hg19) ; chr6:g.160585045C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160585045C>T , CM000668.2:g.160585045C>T	GRCh38
NC_000006.11:g.161006077C>T , CM000668.1:g.161006077C>T	GRCh37
NC_000006.10:g.160926067C>T	NCBI36
NG_016147.1:g.86331G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.4289+1G>A MANE Select	ENSP00000321334.6:n.4289+1G>A
ENST00000316300.9:c.4289+1G>A	ENSP00000321334.5:n.4289+1G>A
NM_005577.2:c.4289+1G>A	NP_005568.2:n.4289+1G>A
NM_005577.3:c.4289+1G>A	NP_005568.2:n.4289+1G>A
NM_005577.4:c.4289+1G>A MANE Select	NP_005568.2:n.4289+1G>A