Canonical Allele Identifier: CA392098855

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43544968A>T (hg19) ; chr15:g.43252770A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252770A>T , CM000677.2:g.43252770A>T	GRCh38
NC_000015.9:g.43544968A>T , CM000677.1:g.43544968A>T	GRCh37
NC_000015.8:g.41332260A>T	NCBI36
NG_016124.1:g.19088T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.851T>A MANE Select	ENSP00000220420.5:p.Val284Asp
ENST00000635871.1:n.320T>A
ENST00000220420.9:c.851T>A	ENSP00000220420.5:p.Val284Asp
ENST00000349114.8:c.605T>A	ENSP00000220419.8:p.Val202Asp
ENST00000610827.4:c.848T>A	ENSP00000479732.1:p.Val283Asp
ENST00000611276.4:c.602T>A	ENSP00000482542.1:p.Val201Asp
ENST00000622115.1:c.854T>A	ENSP00000479638.1:p.Val285Asp
NM_004245.3:c.605T>A	NP_004236.1:p.Val202Asp
NM_201631.3:c.851T>A	NP_963925.2:p.Val284Asp
XM_011522229.1:c.851T>A	XP_011520531.1:p.Val284Asp
XR_931948.1:n.1025T>A
NM_004245.4:c.605T>A	NP_004236.1:p.Val202Asp
NM_201631.4:c.851T>A MANE Select	NP_963925.2:p.Val284Asp