Canonical Allele Identifier: CA2173102641

Gene: TGM5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252842_43252843delinsGC , CM000677.2:g.43252842_43252843delinsGC	GRCh38
NC_000015.9:g.43545040_43545041delinsGC , CM000677.1:g.43545040_43545041delinsGC	GRCh37
NC_000015.8:g.41332332_41332333delinsGC	NCBI36
NG_016124.1:g.19015_19016delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.778_779delinsGC MANE Select	ENSP00000220420.5:p.Ala260=
ENST00000635871.1:n.247_248delinsGC
ENST00000220420.9:c.778_779delinsGC	ENSP00000220420.5:p.Ala260=
ENST00000349114.8:c.532_533delinsGC	ENSP00000220419.8:p.Ala178=
ENST00000610827.4:c.775_776delinsGC	ENSP00000479732.1:p.Ala259=
ENST00000611276.4:c.529_530delinsGC	ENSP00000482542.1:p.Ala177=
ENST00000622115.1:c.781_782delinsGC	ENSP00000479638.1:p.Ala261=
NM_004245.3:c.532_533delinsGC	NP_004236.1:p.Ala178=
NM_201631.3:c.778_779delinsGC	NP_963925.2:p.Ala260=
XM_011522229.1:c.778_779delinsGC	XP_011520531.1:p.Ala260=
XR_931948.1:n.952_953delinsGC
NM_004245.4:c.532_533delinsGC	NP_004236.1:p.Ala178=
NM_201631.4:c.778_779delinsGC MANE Select	NP_963925.2:p.Ala260=