Canonical Allele Identifier: CA2173105902

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43260154C= , CM000677.2:g.43260154C=	GRCh38
NC_000015.9:g.43552352C= , CM000677.1:g.43552352C=	GRCh37
NC_000015.8:g.41339644C=	NCBI36
NG_016124.1:g.11704G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.334G= MANE Select	ENSP00000220420.5:p.Val112=
ENST00000220420.9:c.334G=	ENSP00000220420.5:p.Val112=
ENST00000349114.8:c.190+246G=	ENSP00000220419.8:n.190+246G=
ENST00000610827.4:c.331G=	ENSP00000479732.1:p.Val111=
ENST00000611276.4:c.187+246G=	ENSP00000482542.1:n.187+246G=
ENST00000622115.1:c.337G=	ENSP00000479638.1:p.Val113=
NM_004245.3:c.190+246G=	NP_004236.1:n.190+246G=
NM_201631.3:c.334G=	NP_963925.2:p.Val112=
XM_011522229.1:c.334G=	XP_011520531.1:p.Val112=
XR_931948.1:n.508G=
NM_004245.4:c.190+246G=	NP_004236.1:n.190+246G=
NM_201631.4:c.334G= MANE Select	NP_963925.2:p.Val112=