Canonical Allele Identifier: CA14145884

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58563834T>C , CM000677.2:g.58563834T>C	GRCh38
NC_000015.9:g.58856033T>C , CM000677.1:g.58856033T>C	GRCh37
NC_000015.8:g.56643325T>C	NCBI36
NG_011465.1:g.136859T>C
NG_011465.2:g.136859T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.1388+111T>C MANE Select	ENSP00000299022.5:n.1388+111T>C
ENST00000299022.9:c.1388+111T>C	ENSP00000299022.5:n.1388+111T>C
ENST00000356113.10:c.1388+111T>C	ENSP00000348425.6:n.1388+111T>C
ENST00000414170.7:c.1388+111T>C	ENSP00000395569.3:n.1388+111T>C
ENST00000433326.2:c.1205+111T>C	ENSP00000395002.2:n.1205+111T>C
ENST00000559845.5:n.1356T>C
NM_000236.2:c.1388+111T>C	NP_000227.2:n.1388+111T>C
XM_005254372.1:c.1388+111T>C	XP_005254429.1:n.1388+111T>C
XM_005254374.3:c.1325+111T>C	XP_005254431.1:n.1325+111T>C
XM_006720502.2:c.1247+111T>C	XP_006720565.1:n.1247+111T>C
XM_005254374.4:c.1424+111T>C	XP_005254431.2:n.1424+111T>C
XM_006720502.4:c.1247+111T>C	XP_006720565.1:n.1247+111T>C
XM_024449916.1:c.1388+111T>C	XP_024305684.1:n.1388+111T>C
XM_024449917.1:c.1388+111T>C	XP_024305685.1:n.1388+111T>C
NM_000236.3:c.1388+111T>C MANE Select	NP_000227.2:n.1388+111T>C