Canonical Allele Identifier: CA224979332
Gene: LIPT2 HGNC NCBI
LIPT2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74493632G>A , CM000673.2:g.74493632G>A GRCh38
NC_000011.9:g.74204677G>A , CM000673.1:g.74204677G>A GRCh37
NC_000011.8:g.73882325G>A NCBI36
NG_051333.1:g.5082C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001144869.3:c.72C>T (LIPT2) MANE Select NP_001138341.1:p.Asp24=
ENST00000310109.5:c.72C>T (LIPT2) MANE Select ENSP00000309463.4:p.Asp24=
NM_001144869.1:c.72C>T (LIPT2) NP_001138341.1:p.Asp24=
NM_001144869.2:c.72C>T (LIPT2) NP_001138341.1:p.Asp24=
NM_001319240.1:c.-599G>A (LIPT2-AS1) NP_001306169.1:n.-599G>A
NM_001329941.1:c.72C>T (LIPT2) NP_001316870.1:p.Asp24=
NM_001329941.2:c.72C>T (LIPT2) NP_001316870.1:p.Asp24=
NM_001329942.1:c.72C>T (LIPT2) NP_001316871.1:p.Asp24=
NM_001329942.2:c.72C>T (LIPT2) NP_001316871.1:p.Asp24=
NR_171028.1:n.253G>A (LIPT2-AS1)
ENST00000310109.4:c.72C>T (LIPT2) ENSP00000309463.4:p.Asp24=
ENST00000528085.1:c.16C>T (LIPT2)
XM_011545021.1:c.72C>T (LIPT2) XP_011543323.1:p.Asp24=
XR_132892.1:n.193G>A (LIPT2-AS1)