Canonical Allele Identifier: CA406101240
Community Standard Title: NM_005357.4(LIPE):c.1559C>T (p.Pro520Leu)
Gene: LIPE HGNC NCBI
LIPE-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42408073G>A , CM000681.2:g.42408073G>A GRCh38
NC_000019.9:g.42912225G>A , CM000681.1:g.42912225G>A GRCh37
NC_000019.8:g.47604065G>A NCBI36
NG_034246.1:g.24354C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005357.4:c.1559C>T (LIPE) MANE Select NP_005348.2:p.Pro520Leu
ENST00000244289.9:c.1559C>T (LIPE) MANE Select ENSP00000244289.3:p.Pro520Leu
NM_005357.3:c.1559C>T (LIPE) NP_005348.2:p.Pro520Leu
NR_073180.1:n.77+10849G>A (LIPE-AS1)
NR_126041.1:n.98-185G>A
ENST00000244289.8:c.1559C>T (LIPE) ENSP00000244289.3:p.Pro520Leu
ENST00000602000.1:n.370C>T (LIPE)
XM_005258937.3:c.1559C>T (LIPE) XP_005258994.1:p.Pro520Leu
XM_005258938.3:c.794C>T (LIPE) XP_005258995.1:p.Pro265Leu
XM_005258938.5:c.794C>T (LIPE) XP_005258995.1:p.Pro265Leu
XM_005258939.3:c.845C>T (LIPE) XP_005258996.2:p.Pro282Leu
XM_005258940.3:c.656C>T (LIPE) XP_005258997.1:p.Pro219Leu
XM_005258941.3:c.656C>T (LIPE) XP_005258998.1:p.Pro219Leu
XM_006723218.2:c.656C>T (LIPE) XP_006723281.1:p.Pro219Leu
XM_006723218.3:c.656C>T (LIPE) XP_006723281.1:p.Pro219Leu
XM_017026810.1:c.656C>T (LIPE) XP_016882299.1:p.Pro219Leu
XM_024451514.1:c.794C>T (LIPE) XP_024307282.1:p.Pro265Leu