Canonical Allele Identifier: CA2173102603

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252767A= , CM000677.2:g.43252767A=	GRCh38
NC_000015.9:g.43544965A= , CM000677.1:g.43544965A=	GRCh37
NC_000015.8:g.41332257A=	NCBI36
NG_016124.1:g.19091T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.854T= MANE Select	ENSP00000220420.5:p.Met285=
ENST00000635871.1:n.323T=
ENST00000220420.9:c.854T=	ENSP00000220420.5:p.Met285=
ENST00000349114.8:c.608T=	ENSP00000220419.8:p.Met203=
ENST00000610827.4:c.851T=	ENSP00000479732.1:p.Met284=
ENST00000611276.4:c.605T=	ENSP00000482542.1:p.Met202=
ENST00000622115.1:c.857T=	ENSP00000479638.1:p.Met286=
NM_004245.3:c.608T=	NP_004236.1:p.Met203=
NM_201631.3:c.854T=	NP_963925.2:p.Met285=
XM_011522229.1:c.854T=	XP_011520531.1:p.Met285=
XR_931948.1:n.1028T=
NM_004245.4:c.608T=	NP_004236.1:p.Met203=
NM_201631.4:c.854T= MANE Select	NP_963925.2:p.Met285=