Canonical Allele Identifier: CA2180403458

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58548387C= , CM000677.2:g.58548387C=	GRCh38
NC_000015.9:g.58840586C= , CM000677.1:g.58840586C=	GRCh37
NC_000015.8:g.56627878C=	NCBI36
NG_011465.1:g.121412C=
NG_011465.2:g.121412C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.866C= MANE Select	NP_000227.2:p.Ser289=
ENST00000299022.10:c.866C= MANE Select	ENSP00000299022.5:p.Ser289=
NM_000236.2:c.866C=	NP_000227.2:p.Ser289=
ENST00000299022.9:c.866C=	ENSP00000299022.5:p.Ser289=
ENST00000356113.10:c.866C=	ENSP00000348425.6:p.Ser289=
ENST00000414170.7:c.866C=	ENSP00000395569.3:p.Ser289=
ENST00000433326.2:c.683C=	ENSP00000395002.2:p.Ser228=
ENST00000559845.5:n.723C=
ENST00000560664.1:n.630C=
XM_005254372.1:c.866C=	XP_005254429.1:p.Ser289=
XM_005254374.3:c.803C=	XP_005254431.1:p.Ser268=
XM_005254374.4:c.902C=	XP_005254431.2:p.Ser301=
XM_006720502.2:c.725C=	XP_006720565.1:p.Ser242=
XM_006720502.4:c.725C=	XP_006720565.1:p.Ser242=
XM_011521551.1:c.866C=	XP_011519853.1:p.Ser289=
XM_017022176.1:c.902C=	XP_016877665.1:p.Ser301=
XM_024449916.1:c.866C=	XP_024305684.1:p.Ser289=
XM_024449917.1:c.866C=	XP_024305685.1:p.Ser289=