Canonical Allele Identifier: CA271701183

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58548773T>G , CM000677.2:g.58548773T>G	GRCh38
NC_000015.9:g.58840972T>G , CM000677.1:g.58840972T>G	GRCh37
NC_000015.8:g.56628264T>G	NCBI36
NG_011465.1:g.121798T>G
NG_011465.2:g.121798T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.1051+201T>G MANE Select	NP_000227.2:n.1051+201T>G
ENST00000299022.10:c.1051+201T>G MANE Select	ENSP00000299022.5:n.1051+201T>G
NM_000236.2:c.1051+201T>G	NP_000227.2:n.1051+201T>G
ENST00000299022.9:c.1051+201T>G	ENSP00000299022.5:n.1051+201T>G
ENST00000356113.10:c.1051+201T>G	ENSP00000348425.6:n.1051+201T>G
ENST00000414170.7:c.1051+201T>G	ENSP00000395569.3:n.1051+201T>G
ENST00000433326.2:c.868+201T>G	ENSP00000395002.2:n.868+201T>G
ENST00000559845.5:n.908+201T>G
XM_005254372.1:c.1051+201T>G	XP_005254429.1:n.1051+201T>G
XM_005254374.3:c.988+201T>G	XP_005254431.1:n.988+201T>G
XM_005254374.4:c.1087+201T>G	XP_005254431.2:n.1087+201T>G
XM_006720502.2:c.910+201T>G	XP_006720565.1:n.910+201T>G
XM_006720502.4:c.910+201T>G	XP_006720565.1:n.910+201T>G
XM_011521551.1:c.1051+201T>G	XP_011519853.1:n.1051+201T>G
XM_017022176.1:c.1087+201T>G	XP_016877665.1:n.1087+201T>G
XM_024449916.1:c.1051+201T>G	XP_024305684.1:n.1051+201T>G
XM_024449917.1:c.1051+201T>G	XP_024305685.1:n.1051+201T>G