Canonical Allele Identifier: CA392100119

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545133A>G (hg19) ; chr15:g.43252935A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252935A>G , CM000677.2:g.43252935A>G	GRCh38
NC_000015.9:g.43545133A>G , CM000677.1:g.43545133A>G	GRCh37
NC_000015.8:g.41332425A>G	NCBI36
NG_016124.1:g.18923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.686T>C MANE Select	ENSP00000220420.5:p.Ile229Thr
ENST00000635871.1:n.155T>C
ENST00000220420.9:c.686T>C	ENSP00000220420.5:p.Ile229Thr
ENST00000349114.8:c.440T>C	ENSP00000220419.8:p.Ile147Thr
ENST00000610827.4:c.683T>C	ENSP00000479732.1:p.Ile228Thr
ENST00000611276.4:c.437T>C	ENSP00000482542.1:p.Ile146Thr
ENST00000622115.1:c.689T>C	ENSP00000479638.1:p.Ile230Thr
NM_004245.3:c.440T>C	NP_004236.1:p.Ile147Thr
NM_201631.3:c.686T>C	NP_963925.2:p.Ile229Thr
XM_011522229.1:c.686T>C	XP_011520531.1:p.Ile229Thr
XR_931948.1:n.860T>C
NM_004245.4:c.440T>C	NP_004236.1:p.Ile147Thr
NM_201631.4:c.686T>C MANE Select	NP_963925.2:p.Ile229Thr