Canonical Allele Identifier: CA2519012268
Gene: LIPE HGNC NCBI
LIPE-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.42401858_42401859insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT , CM000681.2:g.42401858_42401859insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT GRCh38
NC_000019.9:g.42906010_42906011insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT , CM000681.1:g.42906010_42906011insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT GRCh37
NC_000019.8:g.47597850_47597851insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT NCBI36
NG_034246.1:g.30605_30606insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000244289.9:c.3221_3222insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) MANE Select ENSP00000244289.3:p.Gly1075ArgfsTer7
ENST00000244289.8:c.3221_3222insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) ENSP00000244289.3:p.Gly1075ArgfsTer7
ENST00000597620.5:c.909_910insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE)
NM_005357.3:c.3221_3222insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) NP_005348.2:p.Gly1075ArgfsTer7
NR_073180.1:n.77+4634_77+4635insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT (LIPE-AS1)
NR_126041.1:n.97+4634_97+4635insACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCTACCCCCGCAGCCCCCGTCT
XM_005258937.3:c.2993_2994insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258994.1:p.Gly999ArgfsTer7
XM_005258938.3:c.2456_2457insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258995.1:p.Gly820ArgfsTer7
XM_005258939.3:c.2507_2508insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258996.2:p.Gly837ArgfsTer7
XM_005258940.3:c.2318_2319insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258997.1:p.Gly774ArgfsTer7
XM_005258941.3:c.2318_2319insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258998.1:p.Gly774ArgfsTer7
XM_006723218.2:c.2318_2319insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_006723281.1:p.Gly774ArgfsTer7
XM_005258938.5:c.2456_2457insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_005258995.1:p.Gly820ArgfsTer7
XM_006723218.3:c.2318_2319insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_006723281.1:p.Gly774ArgfsTer7
XM_017026810.1:c.2318_2319insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_016882299.1:p.Gly774ArgfsTer7
XM_024451514.1:c.2228_2229insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) XP_024307282.1:p.Gly744ArgfsTer7
NM_005357.4:c.3221_3222insTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGGTAGACGGGGGCTGCGGGGG (LIPE) MANE Select NP_005348.2:p.Gly1075ArgfsTer7