Canonical Allele Identifier: CA2173102600

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252764C= , CM000677.2:g.43252764C=	GRCh38
NC_000015.9:g.43544962C= , CM000677.1:g.43544962C=	GRCh37
NC_000015.8:g.41332254C=	NCBI36
NG_016124.1:g.19094G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.857G= MANE Select	ENSP00000220420.5:p.Cys286=
ENST00000635871.1:n.326G=
ENST00000220420.9:c.857G=	ENSP00000220420.5:p.Cys286=
ENST00000349114.8:c.611G=	ENSP00000220419.8:p.Cys204=
ENST00000610827.4:c.854G=	ENSP00000479732.1:p.Cys285=
ENST00000611276.4:c.608G=	ENSP00000482542.1:p.Cys203=
ENST00000622115.1:c.860G=	ENSP00000479638.1:p.Cys287=
NM_004245.3:c.611G=	NP_004236.1:p.Cys204=
NM_201631.3:c.857G=	NP_963925.2:p.Cys286=
XM_011522229.1:c.857G=	XP_011520531.1:p.Cys286=
XR_931948.1:n.1031G=
NM_004245.4:c.611G=	NP_004236.1:p.Cys204=
NM_201631.4:c.857G= MANE Select	NP_963925.2:p.Cys286=