Canonical Allele Identifier: CA392100933

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545760T>C (hg19) ; chr15:g.43253562T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253562T>C , CM000677.2:g.43253562T>C	GRCh38
NC_000015.9:g.43545760T>C , CM000677.1:g.43545760T>C	GRCh37
NC_000015.8:g.41333052T>C	NCBI36
NG_016124.1:g.18296A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.628A>G MANE Select	ENSP00000220420.5:p.Thr210Ala
ENST00000635871.1:n.97A>G
ENST00000220420.9:c.628A>G	ENSP00000220420.5:p.Thr210Ala
ENST00000349114.8:c.382A>G	ENSP00000220419.8:p.Thr128Ala
ENST00000610827.4:c.625A>G	ENSP00000479732.1:p.Thr209Ala
ENST00000611276.4:c.379A>G	ENSP00000482542.1:p.Thr127Ala
ENST00000622115.1:c.631A>G	ENSP00000479638.1:p.Thr211Ala
NM_004245.3:c.382A>G	NP_004236.1:p.Thr128Ala
NM_201631.3:c.628A>G	NP_963925.2:p.Thr210Ala
XM_011522229.1:c.628A>G	XP_011520531.1:p.Thr210Ala
XR_931948.1:n.802A>G
NM_004245.4:c.382A>G	NP_004236.1:p.Thr128Ala
NM_201631.4:c.628A>G MANE Select	NP_963925.2:p.Thr210Ala