Canonical Allele Identifier: CA2628101493
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253695del , CM000677.2:g.43253695del GRCh38
NC_000015.9:g.43545893del , CM000677.1:g.43545893del GRCh37
NC_000015.8:g.41333185del NCBI36
NG_016124.1:g.18167del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.556-57del MANE Select ENSP00000220420.5:n.556-57del
ENST00000220420.9:c.556-57del ENSP00000220420.5:n.556-57del
ENST00000349114.8:c.310-57del ENSP00000220419.8:n.310-57del
ENST00000610827.4:c.553-57del ENSP00000479732.1:n.553-57del
ENST00000611276.4:c.307-57del ENSP00000482542.1:n.307-57del
ENST00000622115.1:c.559-57del ENSP00000479638.1:n.559-57del
NM_004245.3:c.310-57del NP_004236.1:n.310-57del
NM_201631.3:c.556-57del NP_963925.2:n.556-57del
XM_011522229.1:c.556-57del XP_011520531.1:n.556-57del
XR_931948.1:n.730-57del
NM_004245.4:c.310-57del NP_004236.1:n.310-57del
NM_201631.4:c.556-57del MANE Select NP_963925.2:n.556-57del