Canonical Allele Identifier: CA1677111844

Gene: LPA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160548613G= , CM000668.2:g.160548613G=	GRCh38
NC_000006.11:g.160969645G= , CM000668.1:g.160969645G=	GRCh37
NC_000006.10:g.160889635G=	NCBI36
NG_016147.1:g.122763C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5020C= MANE Select	ENSP00000321334.6:p.Pro1674=
ENST00000316300.9:c.5020C=	ENSP00000321334.5:p.Pro1674=
NM_005577.2:c.5020C=	NP_005568.2:p.Pro1674=
NM_005577.3:c.5020C=	NP_005568.2:p.Pro1674=
NM_005577.4:c.5020C= MANE Select	NP_005568.2:p.Pro1674=