Canonical Allele Identifier: CA1677107692

Gene: LPA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160541482C= , CM000668.2:g.160541482C=	GRCh38
NC_000006.11:g.160962514C= , CM000668.1:g.160962514C=	GRCh37
NC_000006.10:g.160882504C=	NCBI36
NG_016147.1:g.129894G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000316300.10:c.5520-301G= MANE Select	ENSP00000321334.6:n.5520-301G=
ENST00000316300.9:c.5520-301G=	ENSP00000321334.5:n.5520-301G=
NM_005577.2:c.5520-301G=	NP_005568.2:n.5520-301G=
NM_005577.3:c.5520-301G=	NP_005568.2:n.5520-301G=
NM_005577.4:c.5520-301G= MANE Select	NP_005568.2:n.5520-301G=