Canonical Allele Identifier: CA1677107699
Gene: LPA HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160541495C= , CM000668.2:g.160541495C= GRCh38
NC_000006.11:g.160962527C= , CM000668.1:g.160962527C= GRCh37
NC_000006.10:g.160882517C= NCBI36
NG_016147.1:g.129881G=

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.5520-314G= MANE Select ENSP00000321334.6:n.5520-314G=
ENST00000316300.9:c.5520-314G= ENSP00000321334.5:n.5520-314G=
NM_005577.2:c.5520-314G= NP_005568.2:n.5520-314G=
NM_005577.3:c.5520-314G= NP_005568.2:n.5520-314G=
NM_005577.4:c.5520-314G= MANE Select NP_005568.2:n.5520-314G=
Search 100 bp 5'
Search 100 bp 3'