Canonical Allele Identifier: CA7585116

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58560910A>G , CM000677.2:g.58560910A>G	GRCh38
NC_000015.9:g.58853109A>G , CM000677.1:g.58853109A>G	GRCh37
NC_000015.8:g.56640401A>G	NCBI36
NG_011465.1:g.133935A>G
NG_011465.2:g.133935A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.1098A>G MANE Select	ENSP00000299022.5:p.Thr366=
ENST00000299022.9:c.1098A>G	ENSP00000299022.5:p.Thr366=
ENST00000356113.10:c.1098A>G	ENSP00000348425.6:p.Thr366=
ENST00000414170.7:c.1098A>G	ENSP00000395569.3:p.Thr366=
ENST00000433326.2:c.915A>G	ENSP00000395002.2:p.Thr305=
ENST00000559845.5:n.955A>G
NM_000236.2:c.1098A>G	NP_000227.2:p.Thr366=
XM_005254372.1:c.1098A>G	XP_005254429.1:p.Thr366=
XM_005254374.3:c.1035A>G	XP_005254431.1:p.Thr345=
XM_006720502.2:c.957A>G	XP_006720565.1:p.Thr319=
XM_005254374.4:c.1134A>G	XP_005254431.2:p.Thr378=
XM_006720502.4:c.957A>G	XP_006720565.1:p.Thr319=
XM_024449916.1:c.1098A>G	XP_024305684.1:p.Thr366=
XM_024449917.1:c.1098A>G	XP_024305685.1:p.Thr366=
NM_000236.3:c.1098A>G MANE Select	NP_000227.2:p.Thr366=