Canonical Allele Identifier: CA2628678306

Gene: LIPC ALDH1A2 LIPC-AS1

Linked Data

• gnomAD v4: 15-58454635-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58454635A>G , CM000677.2:g.58454635A>G	GRCh38
NC_000015.9:g.58746834A>G , CM000677.1:g.58746834A>G	GRCh37
NC_000015.8:g.56534126A>G	NCBI36
NG_011465.1:g.27660A>G
NG_011465.2:g.27660A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.88+22515A>G (LIPC) MANE Select	ENSP00000299022.5:n.88+22515A>G
ENST00000299022.9:c.88+22515A>G (LIPC)	ENSP00000299022.5:n.88+22515A>G
ENST00000356113.10:c.88+22515A>G (LIPC)	ENSP00000348425.6:n.88+22515A>G
ENST00000414170.7:c.88+22515A>G (LIPC)	ENSP00000395569.3:n.88+22515A>G
ENST00000433326.2:c.88+22515A>G (LIPC)	ENSP00000395002.2:n.88+22515A>G
ENST00000558239.5:c.-307+18996T>C (ALDH1A2)	ENSP00000453292.1:n.-307+18996T>C
ENST00000559845.5:n.130+22515A>G (LIPC)
ENST00000560863.5:n.280+18996T>C (ALDH1A2)
NM_000236.2:c.88+22515A>G (LIPC)	NP_000227.2:n.88+22515A>G
NR_120338.1:n.209-17723T>C (LIPC-AS1)
XM_005254372.1:c.88+22515A>G (LIPC)	XP_005254429.1:n.88+22515A>G
XM_011521551.1:c.88+22515A>G (LIPC)	XP_011519853.1:n.88+22515A>G
XM_024449916.1:c.88+22515A>G (LIPC)	XP_024305684.1:n.88+22515A>G
XM_024449917.1:c.88+22515A>G (LIPC)	XP_024305685.1:n.88+22515A>G
NM_000236.3:c.88+22515A>G (LIPC) MANE Select	NP_000227.2:n.88+22515A>G