Canonical Allele Identifier: CA381977154
Gene: LIPT2 HGNC NCBI
LIPT2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74493652C>T , CM000673.2:g.74493652C>T GRCh38
NC_000011.9:g.74204697C>T , CM000673.1:g.74204697C>T GRCh37
NC_000011.8:g.73882345C>T NCBI36
NG_051333.1:g.5062G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310109.5:c.52G>A (LIPT2) MANE Select ENSP00000309463.4:p.Glu18Lys
ENST00000310109.4:c.52G>A (LIPT2) ENSP00000309463.4:p.Glu18Lys
NM_001144869.1:c.52G>A (LIPT2) NP_001138341.1:p.Glu18Lys
XM_011545021.1:c.52G>A (LIPT2) XP_011543323.1:p.Glu18Lys
XR_132892.1:n.213C>T (LIPT2-AS1)
NM_001144869.2:c.52G>A (LIPT2) NP_001138341.1:p.Glu18Lys
NM_001319240.1:c.-579C>T (LIPT2-AS1) NP_001306169.1:n.-579C>T
NM_001329941.1:c.52G>A (LIPT2) NP_001316870.1:p.Glu18Lys
NM_001329942.1:c.52G>A (LIPT2) NP_001316871.1:p.Glu18Lys
NM_001144869.3:c.52G>A (LIPT2) MANE Select NP_001138341.1:p.Glu18Lys
NM_001329941.2:c.52G>A (LIPT2) NP_001316870.1:p.Glu18Lys
NM_001329942.2:c.52G>A (LIPT2) NP_001316871.1:p.Glu18Lys
NR_171028.1:n.273C>T (LIPT2-AS1)