Canonical Allele Identifier: CA714277153

Gene: LIPC ALDH1A2 LIPC-AS1

Linked Data

• dbSNP Id: rs1164783630
• MyVariant Identifiers: chr15:g.58732516C>T (hg19) ; chr15:g.58440317C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58440317C>T , CM000677.2:g.58440317C>T	GRCh38
NC_000015.9:g.58732516C>T , CM000677.1:g.58732516C>T	GRCh37
NC_000015.8:g.56519808C>T	NCBI36
NG_011465.1:g.13342C>T
NG_011465.2:g.13342C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000299022.10:c.88+8197C>T (LIPC) MANE Select	ENSP00000299022.5:n.88+8197C>T
ENST00000299022.9:c.88+8197C>T (LIPC)	ENSP00000299022.5:n.88+8197C>T
ENST00000356113.10:c.88+8197C>T (LIPC)	ENSP00000348425.6:n.88+8197C>T
ENST00000414170.7:c.88+8197C>T (LIPC)	ENSP00000395569.3:n.88+8197C>T
ENST00000433326.2:c.88+8197C>T (LIPC)	ENSP00000395002.2:n.88+8197C>T
ENST00000558239.5:c.-306-20212G>A (ALDH1A2)	ENSP00000453292.1:n.-306-20212G>A
ENST00000559845.5:n.130+8197C>T (LIPC)
ENST00000560863.5:n.281-20212G>A (ALDH1A2)
NM_000236.2:c.88+8197C>T (LIPC)	NP_000227.2:n.88+8197C>T
NR_120338.1:n.209-3405G>A (LIPC-AS1)
XM_005254372.1:c.88+8197C>T (LIPC)	XP_005254429.1:n.88+8197C>T
XM_011521551.1:c.88+8197C>T (LIPC)	XP_011519853.1:n.88+8197C>T
XM_024449916.1:c.88+8197C>T (LIPC)	XP_024305684.1:n.88+8197C>T
XM_024449917.1:c.88+8197C>T (LIPC)	XP_024305685.1:n.88+8197C>T
NM_000236.3:c.88+8197C>T (LIPC) MANE Select	NP_000227.2:n.88+8197C>T