Canonical Allele Identifier: CA392098842
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252767A>T , CM000677.2:g.43252767A>T GRCh38
NC_000015.9:g.43544965A>T , CM000677.1:g.43544965A>T GRCh37
NC_000015.8:g.41332257A>T NCBI36
NG_016124.1:g.19091T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.854T>A MANE Select ENSP00000220420.5:p.Met285Lys
ENST00000635871.1:n.323T>A
ENST00000220420.9:c.854T>A ENSP00000220420.5:p.Met285Lys
ENST00000349114.8:c.608T>A ENSP00000220419.8:p.Met203Lys
ENST00000610827.4:c.851T>A ENSP00000479732.1:p.Met284Lys
ENST00000611276.4:c.605T>A ENSP00000482542.1:p.Met202Lys
ENST00000622115.1:c.857T>A ENSP00000479638.1:p.Met286Lys
NM_004245.3:c.608T>A NP_004236.1:p.Met203Lys
NM_201631.3:c.854T>A NP_963925.2:p.Met285Lys
XM_011522229.1:c.854T>A XP_011520531.1:p.Met285Lys
XR_931948.1:n.1028T>A
NM_004245.4:c.608T>A NP_004236.1:p.Met203Lys
NM_201631.4:c.854T>A MANE Select NP_963925.2:p.Met285Lys