Canonical Allele Identifier: CA1677116121
Gene: LPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160553486_160553489delinsTGTC , CM000668.2:g.160553486_160553489delinsTGTC GRCh38
NC_000006.11:g.160974518_160974521delinsTGTC , CM000668.1:g.160974518_160974521delinsTGTC GRCh37
NC_000006.10:g.160894508_160894511delinsTGTC NCBI36
NG_016147.1:g.117887_117890delinsGACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000316300.10:c.4973+2536_4973+2539delinsGACA MANE Select ENSP00000321334.6:n.4973+2536_4973+2539delinsGACA
ENST00000316300.9:c.4973+2536_4973+2539delinsGACA ENSP00000321334.5:n.4973+2536_4973+2539delinsGACA
NM_005577.2:c.4973+2536_4973+2539delinsGACA NP_005568.2:n.4973+2536_4973+2539delinsGACA
NM_005577.3:c.4973+2536_4973+2539delinsGACA NP_005568.2:n.4973+2536_4973+2539delinsGACA
NM_005577.4:c.4973+2536_4973+2539delinsGACA MANE Select NP_005568.2:n.4973+2536_4973+2539delinsGACA