Canonical Allele Identifier: CA2180350667
Gene: LIPC HGNC NCBI
ALDH1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58432593T>G , CM000677.2:g.58432593T>G GRCh38
NC_000015.9:g.58724792T>G , CM000677.1:g.58724792T>G GRCh37
NC_000015.8:g.56512084T>G NCBI36
NG_011465.1:g.5618T>G
NG_011465.2:g.5618T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299022.10:c.88+473T>G (LIPC) MANE Select ENSP00000299022.5:n.88+473T>G
ENST00000299022.9:c.88+473T>G (LIPC) ENSP00000299022.5:n.88+473T>G
ENST00000356113.10:c.88+473T>G (LIPC) ENSP00000348425.6:n.88+473T>G
ENST00000414170.7:c.88+473T>G (LIPC) ENSP00000395569.3:n.88+473T>G
ENST00000433326.2:c.88+473T>G (LIPC) ENSP00000395002.2:n.88+473T>G
ENST00000558239.5:c.-306-12488A>C (ALDH1A2) ENSP00000453292.1:n.-306-12488A>C
ENST00000559845.5:n.130+473T>G (LIPC)
ENST00000560863.5:n.281-12488A>C (ALDH1A2)
NM_000236.2:c.88+473T>G (LIPC) NP_000227.2:n.88+473T>G
XM_005254372.1:c.88+473T>G (LIPC) XP_005254429.1:n.88+473T>G
XM_011521551.1:c.88+473T>G (LIPC) XP_011519853.1:n.88+473T>G
XM_024449916.1:c.88+473T>G (LIPC) XP_024305684.1:n.88+473T>G
XM_024449917.1:c.88+473T>G (LIPC) XP_024305685.1:n.88+473T>G
NM_000236.3:c.88+473T>G (LIPC) MANE Select NP_000227.2:n.88+473T>G