Canonical Allele Identifier: CA392099990

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545121T>C (hg19) ; chr15:g.43252923T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252923T>C , CM000677.2:g.43252923T>C	GRCh38
NC_000015.9:g.43545121T>C , CM000677.1:g.43545121T>C	GRCh37
NC_000015.8:g.41332413T>C	NCBI36
NG_016124.1:g.18935A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.698A>G MANE Select	ENSP00000220420.5:p.Asp233Gly
ENST00000635871.1:n.167A>G
ENST00000220420.9:c.698A>G	ENSP00000220420.5:p.Asp233Gly
ENST00000349114.8:c.452A>G	ENSP00000220419.8:p.Asp151Gly
ENST00000610827.4:c.695A>G	ENSP00000479732.1:p.Asp232Gly
ENST00000611276.4:c.449A>G	ENSP00000482542.1:p.Asp150Gly
ENST00000622115.1:c.701A>G	ENSP00000479638.1:p.Asp234Gly
NM_004245.3:c.452A>G	NP_004236.1:p.Asp151Gly
NM_201631.3:c.698A>G	NP_963925.2:p.Asp233Gly
XM_011522229.1:c.698A>G	XP_011520531.1:p.Asp233Gly
XR_931948.1:n.872A>G
NM_004245.4:c.452A>G	NP_004236.1:p.Asp151Gly
NM_201631.4:c.698A>G MANE Select	NP_963925.2:p.Asp233Gly