Canonical Allele Identifier: CA7585095

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58560833T>A , CM000677.2:g.58560833T>A	GRCh38
NC_000015.9:g.58853032T>A , CM000677.1:g.58853032T>A	GRCh37
NC_000015.8:g.56640324T>A	NCBI36
NG_011465.1:g.133858T>A
NG_011465.2:g.133858T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.1052-31T>A MANE Select	NP_000227.2:n.1052-31T>A
ENST00000299022.10:c.1052-31T>A MANE Select	ENSP00000299022.5:n.1052-31T>A
NM_000236.2:c.1052-31T>A	NP_000227.2:n.1052-31T>A
ENST00000299022.9:c.1052-31T>A	ENSP00000299022.5:n.1052-31T>A
ENST00000356113.10:c.1052-31T>A	ENSP00000348425.6:n.1052-31T>A
ENST00000414170.7:c.1052-31T>A	ENSP00000395569.3:n.1052-31T>A
ENST00000433326.2:c.869-31T>A	ENSP00000395002.2:n.869-31T>A
ENST00000559845.5:n.909-31T>A
XM_005254372.1:c.1052-31T>A	XP_005254429.1:n.1052-31T>A
XM_005254374.3:c.989-31T>A	XP_005254431.1:n.989-31T>A
XM_005254374.4:c.1088-31T>A	XP_005254431.2:n.1088-31T>A
XM_006720502.2:c.911-31T>A	XP_006720565.1:n.911-31T>A
XM_006720502.4:c.911-31T>A	XP_006720565.1:n.911-31T>A
XM_024449916.1:c.1052-31T>A	XP_024305684.1:n.1052-31T>A
XM_024449917.1:c.1052-31T>A	XP_024305685.1:n.1052-31T>A