Canonical Allele Identifier: CA2180388387

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58520000C= , CM000677.2:g.58520000C=	GRCh38
NC_000015.9:g.58812199C= , CM000677.1:g.58812199C=	GRCh37
NC_000015.8:g.56599491C=	NCBI36
NG_011465.1:g.93025C=
NG_011465.2:g.93025C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.89-18333C= MANE Select	NP_000227.2:n.89-18333C=
ENST00000299022.10:c.89-18333C= MANE Select	ENSP00000299022.5:n.89-18333C=
NM_000236.2:c.89-18333C=	NP_000227.2:n.89-18333C=
ENST00000299022.9:c.89-18333C=	ENSP00000299022.5:n.89-18333C=
ENST00000356113.10:c.89-18333C=	ENSP00000348425.6:n.89-18333C=
ENST00000414170.7:c.89-18333C=	ENSP00000395569.3:n.89-18333C=
ENST00000433326.2:c.89-18333C=	ENSP00000395002.2:n.89-18333C=
ENST00000559845.5:n.131-21785C=
XM_005254372.1:c.89-18333C=	XP_005254429.1:n.89-18333C=
XM_011521551.1:c.89-18333C=	XP_011519853.1:n.89-18333C=
XM_024449916.1:c.89-18333C=	XP_024305684.1:n.89-18333C=
XM_024449917.1:c.89-18333C=	XP_024305685.1:n.89-18333C=