Canonical Allele Identifier: CA1677111841

Gene: LPA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548609C= , CM000668.2:g.160548609C=	GRCh38
NC_000006.11:g.160969641C= , CM000668.1:g.160969641C=	GRCh37
NC_000006.10:g.160889631C=	NCBI36
NG_016147.1:g.122767G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5024G= MANE Select	ENSP00000321334.6:p.Trp1675=
ENST00000316300.9:c.5024G=	ENSP00000321334.5:p.Trp1675=
NM_005577.2:c.5024G=	NP_005568.2:p.Trp1675=
NM_005577.3:c.5024G=	NP_005568.2:p.Trp1675=
NM_005577.4:c.5024G= MANE Select	NP_005568.2:p.Trp1675=