Canonical Allele Identifier: CA1533287
Community Standard Title: NC_000002.12:g.11677686G>C
Gene: LPIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11677686G>C , CM000664.2:g.11677686G>C GRCh38
NC_000002.11:g.11817812G>C , CM000664.1:g.11817812G>C GRCh37
NC_000002.10:g.11735263G>C NCBI36
NG_012843.2:g.5108G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001261428.1:c.39G>C NP_001248357.1:p.Glu13Asp
NM_001261428.2:c.39G>C NP_001248357.1:p.Glu13Asp
NM_001261428.3:c.39G>C NP_001248357.1:p.Glu13Asp
NM_001349207.1:c.39G>C NP_001336136.1:p.Glu13Asp
NM_001349207.2:c.39G>C NP_001336136.1:p.Glu13Asp
NM_001349208.1:c.39G>C NP_001336137.1:p.Glu13Asp
NM_001349208.2:c.39G>C NP_001336137.1:p.Glu13Asp
ENST00000449576.6:c.39G>C ENSP00000397908.2:p.Glu13Asp
XM_006711869.1:c.39G>C XP_006711932.1:p.Glu13Asp
XM_011510333.1:c.39G>C XP_011508635.1:p.Glu13Asp
XM_011510333.2:c.39G>C XP_011508635.1:p.Glu13Asp
XM_011510337.1:c.39G>C XP_011508639.1:p.Glu13Asp
XM_011510338.1:c.39G>C XP_011508640.1:p.Glu13Asp