Canonical Allele Identifier: CA392613741

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58560878T>C , CM000677.2:g.58560878T>C	GRCh38
NC_000015.9:g.58853077T>C , CM000677.1:g.58853077T>C	GRCh37
NC_000015.8:g.56640369T>C	NCBI36
NG_011465.1:g.133903T>C
NG_011465.2:g.133903T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.1066T>C MANE Select	NP_000227.2:p.Phe356Leu
ENST00000299022.10:c.1066T>C MANE Select	ENSP00000299022.5:p.Phe356Leu
NM_000236.2:c.1066T>C	NP_000227.2:p.Phe356Leu
ENST00000299022.9:c.1066T>C	ENSP00000299022.5:p.Phe356Leu
ENST00000356113.10:c.1066T>C	ENSP00000348425.6:p.Phe356Leu
ENST00000414170.7:c.1066T>C	ENSP00000395569.3:p.Phe356Leu
ENST00000433326.2:c.883T>C	ENSP00000395002.2:p.Phe295Leu
ENST00000559845.5:n.923T>C
XM_005254372.1:c.1066T>C	XP_005254429.1:p.Phe356Leu
XM_005254374.3:c.1003T>C	XP_005254431.1:p.Phe335Leu
XM_005254374.4:c.1102T>C	XP_005254431.2:p.Phe368Leu
XM_006720502.2:c.925T>C	XP_006720565.1:p.Phe309Leu
XM_006720502.4:c.925T>C	XP_006720565.1:p.Phe309Leu
XM_024449916.1:c.1066T>C	XP_024305684.1:p.Phe356Leu
XM_024449917.1:c.1066T>C	XP_024305685.1:p.Phe356Leu