Canonical Allele Identifier: CA9476999
Gene: LIPE HGNC NCBI
LIPE-AS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42408224G>A , CM000681.2:g.42408224G>A GRCh38
NC_000019.9:g.42912376G>A , CM000681.1:g.42912376G>A GRCh37
NC_000019.8:g.47604216G>A NCBI36
NG_034246.1:g.24203C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000244289.9:c.1510+8C>T (LIPE) MANE Select ENSP00000244289.3:n.1510+8C>T
ENST00000244289.8:c.1510+8C>T (LIPE) ENSP00000244289.3:n.1510+8C>T
ENST00000599211.1:c.640+8C>T (LIPE) ENSP00000472531.1:n.640+8C>T
ENST00000599783.5:c.745+8C>T (LIPE) ENSP00000469990.1:n.745+8C>T
ENST00000602000.1:n.321+8C>T (LIPE)
NM_005357.3:c.1510+8C>T (LIPE) NP_005348.2:n.1510+8C>T
NR_073180.1:n.77+11000G>A (LIPE-AS1)
NR_126041.1:n.98-34G>A
XM_005258937.3:c.1510+8C>T (LIPE) XP_005258994.1:n.1510+8C>T
XM_005258938.3:c.745+8C>T (LIPE) XP_005258995.1:n.745+8C>T
XM_005258939.3:c.796+8C>T (LIPE) XP_005258996.2:n.796+8C>T
XM_005258940.3:c.607+8C>T (LIPE) XP_005258997.1:n.607+8C>T
XM_005258941.3:c.607+8C>T (LIPE) XP_005258998.1:n.607+8C>T
XM_006723218.2:c.607+8C>T (LIPE) XP_006723281.1:n.607+8C>T
XM_005258938.5:c.745+8C>T (LIPE) XP_005258995.1:n.745+8C>T
XM_006723218.3:c.607+8C>T (LIPE) XP_006723281.1:n.607+8C>T
XM_017026810.1:c.607+8C>T (LIPE) XP_016882299.1:n.607+8C>T
XM_024451514.1:c.745+8C>T (LIPE) XP_024307282.1:n.745+8C>T
NM_005357.4:c.1510+8C>T (LIPE) MANE Select NP_005348.2:n.1510+8C>T