Canonical Allele Identifier: CA271701156

Gene: LIPC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58548723A>T , CM000677.2:g.58548723A>T	GRCh38
NC_000015.9:g.58840922A>T , CM000677.1:g.58840922A>T	GRCh37
NC_000015.8:g.56628214A>T	NCBI36
NG_011465.1:g.121748A>T
NG_011465.2:g.121748A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000236.3:c.1051+151A>T MANE Select	NP_000227.2:n.1051+151A>T
ENST00000299022.10:c.1051+151A>T MANE Select	ENSP00000299022.5:n.1051+151A>T
NM_000236.2:c.1051+151A>T	NP_000227.2:n.1051+151A>T
ENST00000299022.9:c.1051+151A>T	ENSP00000299022.5:n.1051+151A>T
ENST00000356113.10:c.1051+151A>T	ENSP00000348425.6:n.1051+151A>T
ENST00000414170.7:c.1051+151A>T	ENSP00000395569.3:n.1051+151A>T
ENST00000433326.2:c.868+151A>T	ENSP00000395002.2:n.868+151A>T
ENST00000559845.5:n.908+151A>T
XM_005254372.1:c.1051+151A>T	XP_005254429.1:n.1051+151A>T
XM_005254374.3:c.988+151A>T	XP_005254431.1:n.988+151A>T
XM_005254374.4:c.1087+151A>T	XP_005254431.2:n.1087+151A>T
XM_006720502.2:c.910+151A>T	XP_006720565.1:n.910+151A>T
XM_006720502.4:c.910+151A>T	XP_006720565.1:n.910+151A>T
XM_011521551.1:c.1051+151A>T	XP_011519853.1:n.1051+151A>T
XM_017022176.1:c.1087+151A>T	XP_016877665.1:n.1087+151A>T
XM_024449916.1:c.1051+151A>T	XP_024305684.1:n.1051+151A>T
XM_024449917.1:c.1051+151A>T	XP_024305685.1:n.1051+151A>T