Canonical Allele Identifier: CA16507423

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58560590T>G , CM000677.2:g.58560590T>G	GRCh38
NC_000015.9:g.58852789T>G , CM000677.1:g.58852789T>G	GRCh37
NC_000015.8:g.56640081T>G	NCBI36
NG_011465.1:g.133615T>G
NG_011465.2:g.133615T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.1052-274T>G MANE Select	ENSP00000299022.5:n.1052-274T>G
ENST00000299022.9:c.1052-274T>G	ENSP00000299022.5:n.1052-274T>G
ENST00000356113.10:c.1052-274T>G	ENSP00000348425.6:n.1052-274T>G
ENST00000414170.7:c.1052-274T>G	ENSP00000395569.3:n.1052-274T>G
ENST00000433326.2:c.869-274T>G	ENSP00000395002.2:n.869-274T>G
ENST00000559845.5:n.909-274T>G
NM_000236.2:c.1052-274T>G	NP_000227.2:n.1052-274T>G
XM_005254372.1:c.1052-274T>G	XP_005254429.1:n.1052-274T>G
XM_005254374.3:c.989-274T>G	XP_005254431.1:n.989-274T>G
XM_006720502.2:c.911-274T>G	XP_006720565.1:n.911-274T>G
XM_005254374.4:c.1088-274T>G	XP_005254431.2:n.1088-274T>G
XM_006720502.4:c.911-274T>G	XP_006720565.1:n.911-274T>G
XM_024449916.1:c.1052-274T>G	XP_024305684.1:n.1052-274T>G
XM_024449917.1:c.1052-274T>G	XP_024305685.1:n.1052-274T>G
NM_000236.3:c.1052-274T>G MANE Select	NP_000227.2:n.1052-274T>G