Canonical Allele Identifier: CA343578120
Community Standard Title: NM_015602.4(TOR1AIP1):c.349C>T (p.Gln117Ter)
Gene: TOR1AIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179882851C>T , CM000663.2:g.179882851C>T GRCh38
NC_000001.10:g.179851986C>T , CM000663.1:g.179851986C>T GRCh37
NC_000001.9:g.178118609C>T NCBI36
NG_042316.1:g.5810C>T
NG_053185.1:g.764G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015602.4:c.349C>T MANE Select NP_056417.2:p.Gln117Ter
ENST00000606911.7:c.349C>T MANE Select ENSP00000476687.1:p.Gln117Ter
NM_001267578.1:c.349C>T NP_001254507.1:p.Gln117Ter
NM_001267578.2:c.349C>T NP_001254507.1:p.Gln117Ter
NM_015602.3:c.349C>T NP_056417.2:p.Gln117Ter
ENST00000271583.7:c.349C>T ENSP00000271583.3:p.Gln117Ter
ENST00000435319.8:c.-15C>T ENSP00000393292.3:n.-15C>T
ENST00000528443.6:c.349C>T ENSP00000435365.2:p.Gln117Ter
ENST00000531630.6:c.58C>T ENSP00000434316.2:p.Gln20Ter
ENST00000606911.6:c.349C>T ENSP00000476687.1:p.Gln117Ter
XM_011509403.1:c.349C>T XP_011507705.1:p.Gln117Ter
XM_011509403.2:c.349C>T XP_011507705.1:p.Gln117Ter
XM_011509404.1:c.349C>T XP_011507706.1:p.Gln117Ter
XM_011509404.2:c.349C>T XP_011507706.1:p.Gln117Ter