Canonical Allele Identifier: CA2628678314

Gene: LIPC ALDH1A2 LIPC-AS1

Linked Data

• gnomAD v4: 15-58454655-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58454655G>A , CM000677.2:g.58454655G>A	GRCh38
NC_000015.9:g.58746854G>A , CM000677.1:g.58746854G>A	GRCh37
NC_000015.8:g.56534146G>A	NCBI36
NG_011465.1:g.27680G>A
NG_011465.2:g.27680G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000299022.10:c.88+22535G>A (LIPC) MANE Select	ENSP00000299022.5:n.88+22535G>A
ENST00000299022.9:c.88+22535G>A (LIPC)	ENSP00000299022.5:n.88+22535G>A
ENST00000356113.10:c.88+22535G>A (LIPC)	ENSP00000348425.6:n.88+22535G>A
ENST00000414170.7:c.88+22535G>A (LIPC)	ENSP00000395569.3:n.88+22535G>A
ENST00000433326.2:c.88+22535G>A (LIPC)	ENSP00000395002.2:n.88+22535G>A
ENST00000558239.5:c.-307+18976C>T (ALDH1A2)	ENSP00000453292.1:n.-307+18976C>T
ENST00000559845.5:n.130+22535G>A (LIPC)
ENST00000560863.5:n.280+18976C>T (ALDH1A2)
NM_000236.2:c.88+22535G>A (LIPC)	NP_000227.2:n.88+22535G>A
NR_120338.1:n.209-17743C>T (LIPC-AS1)
XM_005254372.1:c.88+22535G>A (LIPC)	XP_005254429.1:n.88+22535G>A
XM_011521551.1:c.88+22535G>A (LIPC)	XP_011519853.1:n.88+22535G>A
XM_024449916.1:c.88+22535G>A (LIPC)	XP_024305684.1:n.88+22535G>A
XM_024449917.1:c.88+22535G>A (LIPC)	XP_024305685.1:n.88+22535G>A
NM_000236.3:c.88+22535G>A (LIPC) MANE Select	NP_000227.2:n.88+22535G>A