Canonical Allele Identifier: CA392099904
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252916A>T , CM000677.2:g.43252916A>T GRCh38
NC_000015.9:g.43545114A>T , CM000677.1:g.43545114A>T GRCh37
NC_000015.8:g.41332406A>T NCBI36
NG_016124.1:g.18942T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.705T>A MANE Select ENSP00000220420.5:p.Asn235Lys
ENST00000635871.1:n.174T>A
ENST00000220420.9:c.705T>A ENSP00000220420.5:p.Asn235Lys
ENST00000349114.8:c.459T>A ENSP00000220419.8:p.Asn153Lys
ENST00000610827.4:c.702T>A ENSP00000479732.1:p.Asn234Lys
ENST00000611276.4:c.456T>A ENSP00000482542.1:p.Asn152Lys
ENST00000622115.1:c.708T>A ENSP00000479638.1:p.Asn236Lys
NM_004245.3:c.459T>A NP_004236.1:p.Asn153Lys
NM_201631.3:c.705T>A NP_963925.2:p.Asn235Lys
XM_011522229.1:c.705T>A XP_011520531.1:p.Asn235Lys
XR_931948.1:n.879T>A
NM_004245.4:c.459T>A NP_004236.1:p.Asn153Lys
NM_201631.4:c.705T>A MANE Select NP_963925.2:p.Asn235Lys