Canonical Allele Identifier: CA490131518

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545078T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252880T>G , CM000677.2:g.43252880T>G	GRCh38
NC_000015.9:g.43545078T>G , CM000677.1:g.43545078T>G	GRCh37
NC_000015.8:g.41332370T>G	NCBI36
NG_016124.1:g.18978A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.741A>C MANE Select	ENSP00000220420.5:p.Thr247=
ENST00000635871.1:n.210A>C
ENST00000220420.9:c.741A>C	ENSP00000220420.5:p.Thr247=
ENST00000349114.8:c.495A>C	ENSP00000220419.8:p.Thr165=
ENST00000610827.4:c.738A>C	ENSP00000479732.1:p.Thr246=
ENST00000611276.4:c.492A>C	ENSP00000482542.1:p.Thr164=
ENST00000622115.1:c.744A>C	ENSP00000479638.1:p.Thr248=
NM_004245.3:c.495A>C	NP_004236.1:p.Thr165=
NM_201631.3:c.741A>C	NP_963925.2:p.Thr247=
XM_011522229.1:c.741A>C	XP_011520531.1:p.Thr247=
XR_931948.1:n.915A>C
NM_004245.4:c.495A>C	NP_004236.1:p.Thr165=
NM_201631.4:c.741A>C MANE Select	NP_963925.2:p.Thr247=