Canonical Allele Identifier: CA1677120456
Gene: LPA HGNC NCBI

Linked Data

dbSNP Id: rs7770628

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160597142C>G , CM000668.2:g.160597142C>G GRCh38
NC_000006.11:g.161018174C>G , CM000668.1:g.161018174C>G GRCh37
NC_000006.10:g.160938164C>G NCBI36
NG_016147.1:g.74234G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316300.10:c.3288-1607G>C MANE Select ENSP00000321334.6:n.3288-1607G>C
ENST00000316300.9:c.3288-1607G>C ENSP00000321334.5:n.3288-1607G>C
ENST00000447678.2:c.1029-1607G>C ENSP00000395608.2:n.1029-1607G>C
NM_005577.2:c.3288-1607G>C NP_005568.2:n.3288-1607G>C
NM_005577.3:c.3288-1607G>C NP_005568.2:n.3288-1607G>C
NM_005577.4:c.3288-1607G>C MANE Select NP_005568.2:n.3288-1607G>C