Canonical Allele Identifier: CA271694092
Gene: LIPC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58542340A>C , CM000677.2:g.58542340A>C GRCh38
NC_000015.9:g.58834539A>C , CM000677.1:g.58834539A>C GRCh37
NC_000015.8:g.56621831A>C NCBI36
NG_011465.1:g.115365A>C
NG_011465.2:g.115365A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000236.3:c.457-194A>C MANE Select NP_000227.2:n.457-194A>C
ENST00000299022.10:c.457-194A>C MANE Select ENSP00000299022.5:n.457-194A>C
NM_000236.2:c.457-194A>C NP_000227.2:n.457-194A>C
ENST00000299022.9:c.457-194A>C ENSP00000299022.5:n.457-194A>C
ENST00000356113.10:c.457-194A>C ENSP00000348425.6:n.457-194A>C
ENST00000414170.7:c.457-194A>C ENSP00000395569.3:n.457-194A>C
ENST00000433326.2:c.274-194A>C ENSP00000395002.2:n.274-194A>C
ENST00000559845.5:n.314-194A>C
ENST00000560664.1:n.221-194A>C
XM_005254372.1:c.457-194A>C XP_005254429.1:n.457-194A>C
XM_005254374.3:c.394-194A>C XP_005254431.1:n.394-194A>C
XM_005254374.4:c.493-194A>C XP_005254431.2:n.493-194A>C
XM_006720502.2:c.316-194A>C XP_006720565.1:n.316-194A>C
XM_006720502.4:c.316-194A>C XP_006720565.1:n.316-194A>C
XM_011521551.1:c.457-194A>C XP_011519853.1:n.457-194A>C
XM_017022176.1:c.493-194A>C XP_016877665.1:n.493-194A>C
XM_024449916.1:c.457-194A>C XP_024305684.1:n.457-194A>C
XM_024449917.1:c.457-194A>C XP_024305685.1:n.457-194A>C