Canonical Allele Identifier: CA2173103041
Gene: TGM5 HGNC NCBI

Linked Data

dbSNP Id: rs2042724019

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253711dup , CM000677.2:g.43253711dup GRCh38
NC_000015.9:g.43545909dup , CM000677.1:g.43545909dup GRCh37
NC_000015.8:g.41333201dup NCBI36
NG_016124.1:g.18152dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.556-72dup MANE Select ENSP00000220420.5:n.556-72dup
ENST00000220420.9:c.556-72dup ENSP00000220420.5:n.556-72dup
ENST00000349114.8:c.310-72dup ENSP00000220419.8:n.310-72dup
ENST00000610827.4:c.553-72dup ENSP00000479732.1:n.553-72dup
ENST00000611276.4:c.307-72dup ENSP00000482542.1:n.307-72dup
ENST00000622115.1:c.559-72dup ENSP00000479638.1:n.559-72dup
NM_004245.3:c.310-72dup NP_004236.1:n.310-72dup
NM_201631.3:c.556-72dup NP_963925.2:n.556-72dup
XM_011522229.1:c.556-72dup XP_011520531.1:n.556-72dup
XR_931948.1:n.730-72dup
NM_004245.4:c.310-72dup NP_004236.1:n.310-72dup
NM_201631.4:c.556-72dup MANE Select NP_963925.2:n.556-72dup