Canonical Allele Identifier: CA1677112024

Gene: LPA

Linked Data

• dbSNP Id: rs1778121872
• gnomAD v4: 6-160548733-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548733T>C , CM000668.2:g.160548733T>C	GRCh38
NC_000006.11:g.160969765T>C , CM000668.1:g.160969765T>C	GRCh37
NC_000006.10:g.160889755T>C	NCBI36
NG_016147.1:g.122643A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.4974-74A>G MANE Select	ENSP00000321334.6:n.4974-74A>G
ENST00000316300.9:c.4974-74A>G	ENSP00000321334.5:n.4974-74A>G
NM_005577.2:c.4974-74A>G	NP_005568.2:n.4974-74A>G
NM_005577.3:c.4974-74A>G	NP_005568.2:n.4974-74A>G
NM_005577.4:c.4974-74A>G MANE Select	NP_005568.2:n.4974-74A>G