Canonical Allele Identifier: CA381976374
Gene: LIPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1422017355

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74493256G>A , CM000673.2:g.74493256G>A GRCh38
NC_000011.9:g.74204301G>A , CM000673.1:g.74204301G>A GRCh37
NC_000011.8:g.73881949G>A NCBI36
NG_051333.1:g.5458C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310109.5:c.448C>T MANE Select ENSP00000309463.4:p.Arg150Cys
ENST00000310109.4:c.448C>T ENSP00000309463.4:p.Arg150Cys
ENST00000527115.1:c.60C>T
ENST00000528085.1:c.181+211C>T
NM_001144869.1:c.448C>T NP_001138341.1:p.Arg150Cys
XM_011545021.1:c.448C>T XP_011543323.1:p.Arg150Cys
NM_001144869.2:c.448C>T NP_001138341.1:p.Arg150Cys
NM_001329941.1:c.448C>T NP_001316870.1:p.Arg150Cys
NM_001329942.1:c.237+211C>T NP_001316871.1:n.237+211C>T
NM_001144869.3:c.448C>T MANE Select NP_001138341.1:p.Arg150Cys
NM_001329941.2:c.448C>T NP_001316870.1:p.Arg150Cys
NM_001329942.2:c.237+211C>T NP_001316871.1:n.237+211C>T