Canonical Allele Identifier: CA366351874

Gene: LPA

Linked Data

• MyVariant Identifiers: chr6:g.160969548A>C (hg19) ; chr6:g.160548516A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548516A>C , CM000668.2:g.160548516A>C	GRCh38
NC_000006.11:g.160969548A>C , CM000668.1:g.160969548A>C	GRCh37
NC_000006.10:g.160889538A>C	NCBI36
NG_016147.1:g.122860T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316300.10:c.5117T>G MANE Select	ENSP00000321334.6:p.Val1706Gly
ENST00000316300.9:c.5117T>G	ENSP00000321334.5:p.Val1706Gly
NM_005577.2:c.5117T>G	NP_005568.2:p.Val1706Gly
NM_005577.3:c.5117T>G	NP_005568.2:p.Val1706Gly
NM_005577.4:c.5117T>G MANE Select	NP_005568.2:p.Val1706Gly