Canonical Allele Identifier: CA2173103057
Gene: TGM5 HGNC NCBI

Linked Data

dbSNP Id: rs2042724208

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43253734A>G , CM000677.2:g.43253734A>G GRCh38
NC_000015.9:g.43545932A>G , CM000677.1:g.43545932A>G GRCh37
NC_000015.8:g.41333224A>G NCBI36
NG_016124.1:g.18124T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.556-100T>C MANE Select ENSP00000220420.5:n.556-100T>C
ENST00000220420.9:c.556-100T>C ENSP00000220420.5:n.556-100T>C
ENST00000349114.8:c.310-100T>C ENSP00000220419.8:n.310-100T>C
ENST00000610827.4:c.553-100T>C ENSP00000479732.1:n.553-100T>C
ENST00000611276.4:c.307-100T>C ENSP00000482542.1:n.307-100T>C
ENST00000622115.1:c.559-100T>C ENSP00000479638.1:n.559-100T>C
NM_004245.3:c.310-100T>C NP_004236.1:n.310-100T>C
NM_201631.3:c.556-100T>C NP_963925.2:n.556-100T>C
XM_011522229.1:c.556-100T>C XP_011520531.1:n.556-100T>C
XR_931948.1:n.730-100T>C
NM_004245.4:c.310-100T>C NP_004236.1:n.310-100T>C
NM_201631.4:c.556-100T>C MANE Select NP_963925.2:n.556-100T>C