Canonical Allele Identifier: CA714287520

Gene: LIPC ALDH1A2 LIPC-AS1

Linked Data

• dbSNP Id: rs1289179177
• gnomAD v3: 15-58454649-G-C
• gnomAD v4: 15-58454649-G-C
• MyVariant Identifiers: chr15:g.58746848G>C (hg19) ; chr15:g.58454649G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58454649G>C , CM000677.2:g.58454649G>C	GRCh38
NC_000015.9:g.58746848G>C , CM000677.1:g.58746848G>C	GRCh37
NC_000015.8:g.56534140G>C	NCBI36
NG_011465.1:g.27674G>C
NG_011465.2:g.27674G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299022.10:c.88+22529G>C (LIPC) MANE Select	ENSP00000299022.5:n.88+22529G>C
ENST00000299022.9:c.88+22529G>C (LIPC)	ENSP00000299022.5:n.88+22529G>C
ENST00000356113.10:c.88+22529G>C (LIPC)	ENSP00000348425.6:n.88+22529G>C
ENST00000414170.7:c.88+22529G>C (LIPC)	ENSP00000395569.3:n.88+22529G>C
ENST00000433326.2:c.88+22529G>C (LIPC)	ENSP00000395002.2:n.88+22529G>C
ENST00000558239.5:c.-307+18982C>G (ALDH1A2)	ENSP00000453292.1:n.-307+18982C>G
ENST00000559845.5:n.130+22529G>C (LIPC)
ENST00000560863.5:n.280+18982C>G (ALDH1A2)
NM_000236.2:c.88+22529G>C (LIPC)	NP_000227.2:n.88+22529G>C
NR_120338.1:n.209-17737C>G (LIPC-AS1)
XM_005254372.1:c.88+22529G>C (LIPC)	XP_005254429.1:n.88+22529G>C
XM_011521551.1:c.88+22529G>C (LIPC)	XP_011519853.1:n.88+22529G>C
XM_024449916.1:c.88+22529G>C (LIPC)	XP_024305684.1:n.88+22529G>C
XM_024449917.1:c.88+22529G>C (LIPC)	XP_024305685.1:n.88+22529G>C
NM_000236.3:c.88+22529G>C (LIPC) MANE Select	NP_000227.2:n.88+22529G>C