Canonical Allele Identifier: CA714272271

Gene: LIPC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58509744A>T , CM000677.2:g.58509744A>T	GRCh38
NC_000015.9:g.58801943A>T , CM000677.1:g.58801943A>T	GRCh37
NC_000015.8:g.56589235A>T	NCBI36
NG_011465.1:g.82769A>T
NG_011465.2:g.82769A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299022.10:c.89-28589A>T MANE Select	ENSP00000299022.5:n.89-28589A>T
ENST00000299022.9:c.89-28589A>T	ENSP00000299022.5:n.89-28589A>T
ENST00000356113.10:c.89-28589A>T	ENSP00000348425.6:n.89-28589A>T
ENST00000414170.7:c.89-28589A>T	ENSP00000395569.3:n.89-28589A>T
ENST00000433326.2:c.89-28589A>T	ENSP00000395002.2:n.89-28589A>T
ENST00000559845.5:n.131-32041A>T
NM_000236.2:c.89-28589A>T	NP_000227.2:n.89-28589A>T
XM_005254372.1:c.89-28589A>T	XP_005254429.1:n.89-28589A>T
XM_011521551.1:c.89-28589A>T	XP_011519853.1:n.89-28589A>T
XM_024449916.1:c.89-28589A>T	XP_024305684.1:n.89-28589A>T
XM_024449917.1:c.89-28589A>T	XP_024305685.1:n.89-28589A>T
NM_000236.3:c.89-28589A>T MANE Select	NP_000227.2:n.89-28589A>T