Canonical Allele Identifier: CA1677111846

Gene: LPA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548615C= , CM000668.2:g.160548615C=	GRCh38
NC_000006.11:g.160969647C= , CM000668.1:g.160969647C=	GRCh37
NC_000006.10:g.160889637C=	NCBI36
NG_016147.1:g.122761G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5018G= MANE Select	ENSP00000321334.6:p.Gly1673=
ENST00000316300.9:c.5018G=	ENSP00000321334.5:p.Gly1673=
NM_005577.2:c.5018G=	NP_005568.2:p.Gly1673=
NM_005577.3:c.5018G=	NP_005568.2:p.Gly1673=
NM_005577.4:c.5018G= MANE Select	NP_005568.2:p.Gly1673=