Canonical Allele Identifier: CA2180350665

Gene: LIPC ALDH1A2

Genomic Alleles

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

Transcript Alleles

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