Canonical Allele Identifier: CA366352314

Gene: LPA

Linked Data

• MyVariant Identifiers: chr6:g.160969650G>C (hg19) ; chr6:g.160548618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548618G>C , CM000668.2:g.160548618G>C	GRCh38
NC_000006.11:g.160969650G>C , CM000668.1:g.160969650G>C	GRCh37
NC_000006.10:g.160889640G>C	NCBI36
NG_016147.1:g.122758C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5015C>G MANE Select	ENSP00000321334.6:p.Thr1672Arg
ENST00000316300.9:c.5015C>G	ENSP00000321334.5:p.Thr1672Arg
NM_005577.2:c.5015C>G	NP_005568.2:p.Thr1672Arg
NM_005577.3:c.5015C>G	NP_005568.2:p.Thr1672Arg
NM_005577.4:c.5015C>G MANE Select	NP_005568.2:p.Thr1672Arg