Canonical Allele Identifier: CA7584798

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58541794G>A , CM000677.2:g.58541794G>A	GRCh38
NC_000015.9:g.58833993G>A , CM000677.1:g.58833993G>A	GRCh37
NC_000015.8:g.56621285G>A	NCBI36
NG_011465.1:g.114819G>A
NG_011465.2:g.114819G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.283G>A MANE Select	ENSP00000299022.5:p.Val95Met
ENST00000299022.9:c.283G>A	ENSP00000299022.5:p.Val95Met
ENST00000356113.10:c.283G>A	ENSP00000348425.6:p.Val95Met
ENST00000414170.7:c.283G>A	ENSP00000395569.3:p.Val95Met
ENST00000433326.2:c.274-740G>A	ENSP00000395002.2:n.274-740G>A
ENST00000559845.5:n.140G>A
ENST00000560664.1:n.47G>A
NM_000236.2:c.283G>A	NP_000227.2:p.Val95Met
XM_005254372.1:c.283G>A	XP_005254429.1:p.Val95Met
XM_005254374.3:c.220G>A	XP_005254431.1:p.Val74Met
XM_006720502.2:c.142G>A	XP_006720565.1:p.Val48Met
XM_011521551.1:c.283G>A	XP_011519853.1:p.Val95Met
XM_005254374.4:c.319G>A	XP_005254431.2:p.Val107Met
XM_006720502.4:c.142G>A	XP_006720565.1:p.Val48Met
XM_017022176.1:c.319G>A	XP_016877665.1:p.Val107Met
XM_024449916.1:c.283G>A	XP_024305684.1:p.Val95Met
XM_024449917.1:c.283G>A	XP_024305685.1:p.Val95Met
NM_000236.3:c.283G>A MANE Select	NP_000227.2:p.Val95Met