Canonical Allele Identifier: CA2173102966

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253555C= , CM000677.2:g.43253555C=	GRCh38
NC_000015.9:g.43545753C= , CM000677.1:g.43545753C=	GRCh37
NC_000015.8:g.41333045C=	NCBI36
NG_016124.1:g.18303G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.635G= MANE Select	ENSP00000220420.5:p.Cys212=
ENST00000635871.1:n.104G=
ENST00000220420.9:c.635G=	ENSP00000220420.5:p.Cys212=
ENST00000349114.8:c.389G=	ENSP00000220419.8:p.Cys130=
ENST00000610827.4:c.632G=	ENSP00000479732.1:p.Cys211=
ENST00000611276.4:c.386G=	ENSP00000482542.1:p.Cys129=
ENST00000622115.1:c.638G=	ENSP00000479638.1:p.Cys213=
NM_004245.3:c.389G=	NP_004236.1:p.Cys130=
NM_201631.3:c.635G=	NP_963925.2:p.Cys212=
XM_011522229.1:c.635G=	XP_011520531.1:p.Cys212=
XR_931948.1:n.809G=
NM_004245.4:c.389G=	NP_004236.1:p.Cys130=
NM_201631.4:c.635G= MANE Select	NP_963925.2:p.Cys212=