Canonical Allele Identifier: CA15858362

Linked Data

dbSNP Id: rs12593008

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58468776C>A , CM000677.2:g.58468776C>A GRCh38
NC_000015.9:g.58760975C>A , CM000677.1:g.58760975C>A GRCh37
NC_000015.8:g.56548267C>A NCBI36
NG_011465.1:g.41801C>A
NG_011465.2:g.41801C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000299022.10:c.88+36656C>A (LIPC) MANE Select ENSP00000299022.5:n.88+36656C>A
ENST00000299022.9:c.88+36656C>A (LIPC) ENSP00000299022.5:n.88+36656C>A
ENST00000356113.10:c.88+36656C>A (LIPC) ENSP00000348425.6:n.88+36656C>A
ENST00000414170.7:c.88+36656C>A (LIPC) ENSP00000395569.3:n.88+36656C>A
ENST00000433326.2:c.88+36656C>A (LIPC) ENSP00000395002.2:n.88+36656C>A
ENST00000558239.5:c.-307+4855G>T (ALDH1A2) ENSP00000453292.1:n.-307+4855G>T
ENST00000559845.5:n.130+36656C>A (LIPC)
ENST00000560863.5:n.280+4855G>T (ALDH1A2)
NM_000236.2:c.88+36656C>A (LIPC) NP_000227.2:n.88+36656C>A
NR_120338.1:n.208+25997G>T (LIPC-AS1)
XM_005254372.1:c.88+36656C>A (LIPC) XP_005254429.1:n.88+36656C>A
XM_011521551.1:c.88+36656C>A (LIPC) XP_011519853.1:n.88+36656C>A
XM_024449916.1:c.88+36656C>A (LIPC) XP_024305684.1:n.88+36656C>A
XM_024449917.1:c.88+36656C>A (LIPC) XP_024305685.1:n.88+36656C>A
NM_000236.3:c.88+36656C>A (LIPC) MANE Select NP_000227.2:n.88+36656C>A