Canonical Allele Identifier: CA392099406
Gene: TGM5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.43545056A>T (hg19) chr15:g.43252858A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252858A>T , CM000677.2:g.43252858A>T GRCh38
NC_000015.9:g.43545056A>T , CM000677.1:g.43545056A>T GRCh37
NC_000015.8:g.41332348A>T NCBI36
NG_016124.1:g.19000T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000220420.10:c.763T>A MANE Select ENSP00000220420.5:p.Trp255Arg
ENST00000635871.1:n.232T>A
ENST00000220420.9:c.763T>A ENSP00000220420.5:p.Trp255Arg
ENST00000349114.8:c.517T>A ENSP00000220419.8:p.Trp173Arg
ENST00000610827.4:c.760T>A ENSP00000479732.1:p.Trp254Arg
ENST00000611276.4:c.514T>A ENSP00000482542.1:p.Trp172Arg
ENST00000622115.1:c.766T>A ENSP00000479638.1:p.Trp256Arg
NM_004245.3:c.517T>A NP_004236.1:p.Trp173Arg
NM_201631.3:c.763T>A NP_963925.2:p.Trp255Arg
XM_011522229.1:c.763T>A XP_011520531.1:p.Trp255Arg
XR_931948.1:n.937T>A
NM_004245.4:c.517T>A NP_004236.1:p.Trp173Arg
NM_201631.4:c.763T>A MANE Select NP_963925.2:p.Trp255Arg
Search 100 bp 5'
Search 100 bp 3'