Canonical Allele Identifier: CA392099073

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545005G>T (hg19) ; chr15:g.43252807G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252807G>T , CM000677.2:g.43252807G>T	GRCh38
NC_000015.9:g.43545005G>T , CM000677.1:g.43545005G>T	GRCh37
NC_000015.8:g.41332297G>T	NCBI36
NG_016124.1:g.19051C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.814C>A MANE Select	ENSP00000220420.5:p.Pro272Thr
ENST00000635871.1:n.283C>A
ENST00000220420.9:c.814C>A	ENSP00000220420.5:p.Pro272Thr
ENST00000349114.8:c.568C>A	ENSP00000220419.8:p.Pro190Thr
ENST00000610827.4:c.811C>A	ENSP00000479732.1:p.Pro271Thr
ENST00000611276.4:c.565C>A	ENSP00000482542.1:p.Pro189Thr
ENST00000622115.1:c.817C>A	ENSP00000479638.1:p.Pro273Thr
NM_004245.3:c.568C>A	NP_004236.1:p.Pro190Thr
NM_201631.3:c.814C>A	NP_963925.2:p.Pro272Thr
XM_011522229.1:c.814C>A	XP_011520531.1:p.Pro272Thr
XR_931948.1:n.988C>A
NM_004245.4:c.568C>A	NP_004236.1:p.Pro190Thr
NM_201631.4:c.814C>A MANE Select	NP_963925.2:p.Pro272Thr