Canonical Allele Identifier: CA1677112005

Gene: LPA

Linked Data

• dbSNP Id: rs1778121589

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548717A>G , CM000668.2:g.160548717A>G	GRCh38
NC_000006.11:g.160969749A>G , CM000668.1:g.160969749A>G	GRCh37
NC_000006.10:g.160889739A>G	NCBI36
NG_016147.1:g.122659T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.4974-58T>C MANE Select	ENSP00000321334.6:n.4974-58T>C
ENST00000316300.9:c.4974-58T>C	ENSP00000321334.5:n.4974-58T>C
NM_005577.2:c.4974-58T>C	NP_005568.2:n.4974-58T>C
NM_005577.3:c.4974-58T>C	NP_005568.2:n.4974-58T>C
NM_005577.4:c.4974-58T>C MANE Select	NP_005568.2:n.4974-58T>C