Canonical Allele Identifier: CA7585258

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58568764C>A , CM000677.2:g.58568764C>A	GRCh38
NC_000015.9:g.58860963C>A , CM000677.1:g.58860963C>A	GRCh37
NC_000015.8:g.56648255C>A	NCBI36
NG_011465.1:g.141789C>A
NG_011465.2:g.141789C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.1437C>A MANE Select	ENSP00000299022.5:p.Thr479=
ENST00000299022.9:c.1437C>A	ENSP00000299022.5:p.Thr479=
ENST00000356113.10:c.1437C>A	ENSP00000348425.6:p.Thr479=
ENST00000433326.2:c.1254C>A	ENSP00000395002.2:p.Thr418=
NM_000236.2:c.1437C>A	NP_000227.2:p.Thr479=
XM_005254372.1:c.1437C>A	XP_005254429.1:p.Thr479=
XM_005254374.3:c.1374C>A	XP_005254431.1:p.Thr458=
XM_006720502.2:c.1296C>A	XP_006720565.1:p.Thr432=
XM_005254374.4:c.1473C>A	XP_005254431.2:p.Thr491=
XM_006720502.4:c.1296C>A	XP_006720565.1:p.Thr432=
XM_024449916.1:c.1437C>A	XP_024305684.1:p.Thr479=
XM_024449917.1:c.1437C>A	XP_024305685.1:p.Thr479=
NM_000236.3:c.1437C>A MANE Select	NP_000227.2:p.Thr479=