Canonical Allele Identifier: CA392099014

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43544994G>T (hg19) ; chr15:g.43252796G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252796G>T , CM000677.2:g.43252796G>T	GRCh38
NC_000015.9:g.43544994G>T , CM000677.1:g.43544994G>T	GRCh37
NC_000015.8:g.41332286G>T	NCBI36
NG_016124.1:g.19062C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.825C>A MANE Select	ENSP00000220420.5:p.Tyr275Ter
ENST00000635871.1:n.294C>A
ENST00000220420.9:c.825C>A	ENSP00000220420.5:p.Tyr275Ter
ENST00000349114.8:c.579C>A	ENSP00000220419.8:p.Tyr193Ter
ENST00000610827.4:c.822C>A	ENSP00000479732.1:p.Tyr274Ter
ENST00000611276.4:c.576C>A	ENSP00000482542.1:p.Tyr192Ter
ENST00000622115.1:c.828C>A	ENSP00000479638.1:p.Tyr276Ter
NM_004245.3:c.579C>A	NP_004236.1:p.Tyr193Ter
NM_201631.3:c.825C>A	NP_963925.2:p.Tyr275Ter
XM_011522229.1:c.825C>A	XP_011520531.1:p.Tyr275Ter
XR_931948.1:n.999C>A
NM_004245.4:c.579C>A	NP_004236.1:p.Tyr193Ter
NM_201631.4:c.825C>A MANE Select	NP_963925.2:p.Tyr275Ter