Canonical Allele Identifier: CA2628101015
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252957G>T , CM000677.2:g.43252957G>T GRCh38
NC_000015.9:g.43545155G>T , CM000677.1:g.43545155G>T GRCh37
NC_000015.8:g.41332447G>T NCBI36
NG_016124.1:g.18901C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.685-21C>A MANE Select ENSP00000220420.5:n.685-21C>A
ENST00000635871.1:n.154-21C>A
ENST00000220420.9:c.685-21C>A ENSP00000220420.5:n.685-21C>A
ENST00000349114.8:c.439-21C>A ENSP00000220419.8:n.439-21C>A
ENST00000610827.4:c.682-21C>A ENSP00000479732.1:n.682-21C>A
ENST00000611276.4:c.436-21C>A ENSP00000482542.1:n.436-21C>A
ENST00000622115.1:c.688-21C>A ENSP00000479638.1:n.688-21C>A
NM_004245.3:c.439-21C>A NP_004236.1:n.439-21C>A
NM_201631.3:c.685-21C>A NP_963925.2:n.685-21C>A
XM_011522229.1:c.685-21C>A XP_011520531.1:n.685-21C>A
XR_931948.1:n.859-21C>A
NM_004245.4:c.439-21C>A NP_004236.1:n.439-21C>A
NM_201631.4:c.685-21C>A MANE Select NP_963925.2:n.685-21C>A