Canonical Allele Identifier: CA392098836
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252766C>G , CM000677.2:g.43252766C>G GRCh38
NC_000015.9:g.43544964C>G , CM000677.1:g.43544964C>G GRCh37
NC_000015.8:g.41332256C>G NCBI36
NG_016124.1:g.19092G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000220420.10:c.855G>C MANE Select ENSP00000220420.5:p.Met285Ile
ENST00000635871.1:n.324G>C
ENST00000220420.9:c.855G>C ENSP00000220420.5:p.Met285Ile
ENST00000349114.8:c.609G>C ENSP00000220419.8:p.Met203Ile
ENST00000610827.4:c.852G>C ENSP00000479732.1:p.Met284Ile
ENST00000611276.4:c.606G>C ENSP00000482542.1:p.Met202Ile
ENST00000622115.1:c.858G>C ENSP00000479638.1:p.Met286Ile
NM_004245.3:c.609G>C NP_004236.1:p.Met203Ile
NM_201631.3:c.855G>C NP_963925.2:p.Met285Ile
XM_011522229.1:c.855G>C XP_011520531.1:p.Met285Ile
XR_931948.1:n.1029G>C
NM_004245.4:c.609G>C NP_004236.1:p.Met203Ile
NM_201631.4:c.855G>C MANE Select NP_963925.2:p.Met285Ile