Canonical Allele Identifier: CA2173103006
Gene: TGM5 HGNC NCBI

Linked Data

dbSNP Id: rs2042723203

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253638del , CM000677.2:g.43253638del GRCh38
NC_000015.9:g.43545836del , CM000677.1:g.43545836del GRCh37
NC_000015.8:g.41333128del NCBI36
NG_016124.1:g.18220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.556-4del MANE Select ENSP00000220420.5:n.556-4del
ENST00000635871.1:n.21del
ENST00000220420.9:c.556-4del ENSP00000220420.5:n.556-4del
ENST00000349114.8:c.310-4del ENSP00000220419.8:n.310-4del
ENST00000610827.4:c.553-4del ENSP00000479732.1:n.553-4del
ENST00000611276.4:c.307-4del ENSP00000482542.1:n.307-4del
ENST00000622115.1:c.559-4del ENSP00000479638.1:n.559-4del
NM_004245.3:c.310-4del NP_004236.1:n.310-4del
NM_201631.3:c.556-4del NP_963925.2:n.556-4del
XM_011522229.1:c.556-4del XP_011520531.1:n.556-4del
XR_931948.1:n.730-4del
NM_004245.4:c.310-4del NP_004236.1:n.310-4del
NM_201631.4:c.556-4del MANE Select NP_963925.2:n.556-4del