Canonical Allele Identifier: CA381976331
Gene: LIPT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.74493237C>T , CM000673.2:g.74493237C>T GRCh38
NC_000011.9:g.74204282C>T , CM000673.1:g.74204282C>T GRCh37
NC_000011.8:g.73881930C>T NCBI36
NG_051333.1:g.5477G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000310109.5:c.466+1G>A MANE Select ENSP00000309463.4:n.466+1G>A
ENST00000310109.4:c.466+1G>A ENSP00000309463.4:n.466+1G>A
ENST00000527115.1:c.79G>A
ENST00000528085.1:c.181+230G>A
NM_001144869.1:c.466+1G>A NP_001138341.1:n.466+1G>A
XM_011545021.1:c.467G>A XP_011543323.1:p.Gly156Asp
NM_001144869.2:c.466+1G>A NP_001138341.1:n.466+1G>A
NM_001329941.1:c.467G>A NP_001316870.1:p.Gly156Asp
NM_001329942.1:c.237+230G>A NP_001316871.1:n.237+230G>A
NM_001144869.3:c.466+1G>A MANE Select NP_001138341.1:n.466+1G>A
NM_001329941.2:c.467G>A NP_001316870.1:p.Gly156Asp
NM_001329942.2:c.237+230G>A NP_001316871.1:n.237+230G>A