Canonical Allele Identifier: CA2180390148

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58560880C= , CM000677.2:g.58560880C=	GRCh38
NC_000015.9:g.58853079C= , CM000677.1:g.58853079C=	GRCh37
NC_000015.8:g.56640371C=	NCBI36
NG_011465.1:g.133905C=
NG_011465.2:g.133905C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.1068C= MANE Select	NP_000227.2:p.Phe356=
ENST00000299022.10:c.1068C= MANE Select	ENSP00000299022.5:p.Phe356=
NM_000236.2:c.1068C=	NP_000227.2:p.Phe356=
ENST00000299022.9:c.1068C=	ENSP00000299022.5:p.Phe356=
ENST00000356113.10:c.1068C=	ENSP00000348425.6:p.Phe356=
ENST00000414170.7:c.1068C=	ENSP00000395569.3:p.Phe356=
ENST00000433326.2:c.885C=	ENSP00000395002.2:p.Phe295=
ENST00000559845.5:n.925C=
XM_005254372.1:c.1068C=	XP_005254429.1:p.Phe356=
XM_005254374.3:c.1005C=	XP_005254431.1:p.Phe335=
XM_005254374.4:c.1104C=	XP_005254431.2:p.Phe368=
XM_006720502.2:c.927C=	XP_006720565.1:p.Phe309=
XM_006720502.4:c.927C=	XP_006720565.1:p.Phe309=
XM_024449916.1:c.1068C=	XP_024305684.1:p.Phe356=
XM_024449917.1:c.1068C=	XP_024305685.1:p.Phe356=