Canonical Allele Identifier: CA2173102599

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252760T= , CM000677.2:g.43252760T=	GRCh38
NC_000015.9:g.43544958T= , CM000677.1:g.43544958T=	GRCh37
NC_000015.8:g.41332250T=	NCBI36
NG_016124.1:g.19098A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.861A= MANE Select	ENSP00000220420.5:p.Thr287=
ENST00000635871.1:n.330A=
ENST00000220420.9:c.861A=	ENSP00000220420.5:p.Thr287=
ENST00000349114.8:c.615A=	ENSP00000220419.8:p.Thr205=
ENST00000610827.4:c.858A=	ENSP00000479732.1:p.Thr286=
ENST00000611276.4:c.612A=	ENSP00000482542.1:p.Thr204=
ENST00000622115.1:c.864A=	ENSP00000479638.1:p.Thr288=
NM_004245.3:c.615A=	NP_004236.1:p.Thr205=
NM_201631.3:c.861A=	NP_963925.2:p.Thr287=
XM_011522229.1:c.861A=	XP_011520531.1:p.Thr287=
XR_931948.1:n.1035A=
NM_004245.4:c.615A=	NP_004236.1:p.Thr205=
NM_201631.4:c.861A= MANE Select	NP_963925.2:p.Thr287=