Canonical Allele Identifier: CA402422598
Community Standard Title: NM_006033.4(LIPG):c.1158A>G (p.Ile386Met)
Gene: LIPG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49583556A>G , CM000680.2:g.49583556A>G GRCh38
NC_000018.9:g.47109926A>G , CM000680.1:g.47109926A>G GRCh37
NC_000018.8:g.45363924A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006033.4:c.1158A>G MANE Select NP_006024.1:p.Ile386Met
ENST00000261292.9:c.1158A>G MANE Select ENSP00000261292.4:p.Ile386Met
NM_001308006.1:c.936A>G NP_001294935.1:p.Ile312Met
NM_001308006.2:c.936A>G NP_001294935.1:p.Ile312Met
NM_006033.2:c.1158A>G NP_006024.1:p.Ile386Met
NM_006033.3:c.1158A>G NP_006024.1:p.Ile386Met
ENST00000261292.8:c.1158A>G ENSP00000261292.4:p.Ile386Met
ENST00000427224.6:c.936A>G ENSP00000387978.2:p.Ile312Met
XM_005258390.1:c.1266A>G XP_005258447.1:p.Ile422Met
XM_011526265.1:c.1044A>G XP_011524567.1:p.Ile348Met
XM_011526265.3:c.1044A>G XP_011524567.1:p.Ile348Met
XM_011526267.1:c.918A>G XP_011524569.1:p.Ile306Met
XM_017026095.1:c.567A>G XP_016881584.1:p.Ile189Met