Canonical Allele Identifier: CA2173094822

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43238827C= , CM000677.2:g.43238827C=	GRCh38
NC_000015.9:g.43531025C= , CM000677.1:g.43531025C=	GRCh37
NC_000015.8:g.41318317C=	NCBI36
NG_016124.1:g.33031G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.1335G= MANE Select	ENSP00000220420.5:p.Lys445=
ENST00000220420.9:c.1335G=	ENSP00000220420.5:p.Lys445=
ENST00000349114.8:c.1089G=	ENSP00000220419.8:p.Lys363=
ENST00000396996.3:n.811G=
ENST00000610827.4:c.1332G=	ENSP00000479732.1:p.Lys444=
ENST00000611276.4:c.1086G=	ENSP00000482542.1:p.Lys362=
ENST00000622115.1:c.1338G=	ENSP00000479638.1:p.Lys446=
NM_004245.3:c.1089G=	NP_004236.1:p.Lys363=
NM_201631.3:c.1335G=	NP_963925.2:p.Lys445=
XM_011522229.1:c.1335G=	XP_011520531.1:p.Lys445=
XM_011522230.1:c.306G=	XP_011520532.1:p.Lys102=
XR_931948.1:n.1509G=
XM_011522230.2:c.306G=	XP_011520532.1:p.Lys102=
XM_017022729.1:c.306G=	XP_016878218.1:p.Lys102=
NM_004245.4:c.1089G=	NP_004236.1:p.Lys363=
NM_201631.4:c.1335G= MANE Select	NP_963925.2:p.Lys445=