Canonical Allele Identifier: CA2628101480
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253678_43253687del , CM000677.2:g.43253678_43253687del GRCh38
NC_000015.9:g.43545876_43545885del , CM000677.1:g.43545876_43545885del GRCh37
NC_000015.8:g.41333168_41333177del NCBI36
NG_016124.1:g.18172_18181del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.556-52_556-43del MANE Select ENSP00000220420.5:n.556-52_556-43del
ENST00000220420.9:c.556-52_556-43del ENSP00000220420.5:n.556-52_556-43del
ENST00000349114.8:c.310-52_310-43del ENSP00000220419.8:n.310-52_310-43del
ENST00000610827.4:c.553-52_553-43del ENSP00000479732.1:n.553-52_553-43del
ENST00000611276.4:c.307-52_307-43del ENSP00000482542.1:n.307-52_307-43del
ENST00000622115.1:c.559-52_559-43del ENSP00000479638.1:n.559-52_559-43del
NM_004245.3:c.310-52_310-43del NP_004236.1:n.310-52_310-43del
NM_201631.3:c.556-52_556-43del NP_963925.2:n.556-52_556-43del
XM_011522229.1:c.556-52_556-43del XP_011520531.1:n.556-52_556-43del
XR_931948.1:n.730-52_730-43del
NM_004245.4:c.310-52_310-43del NP_004236.1:n.310-52_310-43del
NM_201631.4:c.556-52_556-43del MANE Select NP_963925.2:n.556-52_556-43del