Canonical Allele Identifier: CA2173102697

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252955G= , CM000677.2:g.43252955G=	GRCh38
NC_000015.9:g.43545153G= , CM000677.1:g.43545153G=	GRCh37
NC_000015.8:g.41332445G=	NCBI36
NG_016124.1:g.18903C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.685-19C= MANE Select	ENSP00000220420.5:n.685-19C=
ENST00000635871.1:n.154-19C=
ENST00000220420.9:c.685-19C=	ENSP00000220420.5:n.685-19C=
ENST00000349114.8:c.439-19C=	ENSP00000220419.8:n.439-19C=
ENST00000610827.4:c.682-19C=	ENSP00000479732.1:n.682-19C=
ENST00000611276.4:c.436-19C=	ENSP00000482542.1:n.436-19C=
ENST00000622115.1:c.688-19C=	ENSP00000479638.1:n.688-19C=
NM_004245.3:c.439-19C=	NP_004236.1:n.439-19C=
NM_201631.3:c.685-19C=	NP_963925.2:n.685-19C=
XM_011522229.1:c.685-19C=	XP_011520531.1:n.685-19C=
XR_931948.1:n.859-19C=
NM_004245.4:c.439-19C=	NP_004236.1:n.439-19C=
NM_201631.4:c.685-19C= MANE Select	NP_963925.2:n.685-19C=