Canonical Allele Identifier: CA7584969

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58545898A>G , CM000677.2:g.58545898A>G	GRCh38
NC_000015.9:g.58838097A>G , CM000677.1:g.58838097A>G	GRCh37
NC_000015.8:g.56625389A>G	NCBI36
NG_011465.1:g.118923A>G
NG_011465.2:g.118923A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.731A>G MANE Select	NP_000227.2:p.Tyr244Cys
ENST00000299022.10:c.731A>G MANE Select	ENSP00000299022.5:p.Tyr244Cys
NM_000236.2:c.731A>G	NP_000227.2:p.Tyr244Cys
ENST00000299022.9:c.731A>G	ENSP00000299022.5:p.Tyr244Cys
ENST00000356113.10:c.731A>G	ENSP00000348425.6:p.Tyr244Cys
ENST00000414170.7:c.731A>G	ENSP00000395569.3:p.Tyr244Cys
ENST00000433326.2:c.548A>G	ENSP00000395002.2:p.Tyr183Cys
ENST00000559845.5:n.588A>G
ENST00000560664.1:n.495A>G
XM_005254372.1:c.731A>G	XP_005254429.1:p.Tyr244Cys
XM_005254374.3:c.668A>G	XP_005254431.1:p.Tyr223Cys
XM_005254374.4:c.767A>G	XP_005254431.2:p.Tyr256Cys
XM_006720502.2:c.590A>G	XP_006720565.1:p.Tyr197Cys
XM_006720502.4:c.590A>G	XP_006720565.1:p.Tyr197Cys
XM_011521551.1:c.731A>G	XP_011519853.1:p.Tyr244Cys
XM_017022176.1:c.767A>G	XP_016877665.1:p.Tyr256Cys
XM_024449916.1:c.731A>G	XP_024305684.1:p.Tyr244Cys
XM_024449917.1:c.731A>G	XP_024305685.1:p.Tyr244Cys