Canonical Allele Identifier: CA392099640

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545085T>G (hg19) ; chr15:g.43252887T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252887T>G , CM000677.2:g.43252887T>G	GRCh38
NC_000015.9:g.43545085T>G , CM000677.1:g.43545085T>G	GRCh37
NC_000015.8:g.41332377T>G	NCBI36
NG_016124.1:g.18971A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.734A>C MANE Select	ENSP00000220420.5:p.Asn245Thr
ENST00000635871.1:n.203A>C
ENST00000220420.9:c.734A>C	ENSP00000220420.5:p.Asn245Thr
ENST00000349114.8:c.488A>C	ENSP00000220419.8:p.Asn163Thr
ENST00000610827.4:c.731A>C	ENSP00000479732.1:p.Asn244Thr
ENST00000611276.4:c.485A>C	ENSP00000482542.1:p.Asn162Thr
ENST00000622115.1:c.737A>C	ENSP00000479638.1:p.Asn246Thr
NM_004245.3:c.488A>C	NP_004236.1:p.Asn163Thr
NM_201631.3:c.734A>C	NP_963925.2:p.Asn245Thr
XM_011522229.1:c.734A>C	XP_011520531.1:p.Asn245Thr
XR_931948.1:n.908A>C
NM_004245.4:c.488A>C	NP_004236.1:p.Asn163Thr
NM_201631.4:c.734A>C MANE Select	NP_963925.2:p.Asn245Thr