Canonical Allele Identifier: CA490131437

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43544967G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252769G>T , CM000677.2:g.43252769G>T	GRCh38
NC_000015.9:g.43544967G>T , CM000677.1:g.43544967G>T	GRCh37
NC_000015.8:g.41332259G>T	NCBI36
NG_016124.1:g.19089C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.852C>A MANE Select	ENSP00000220420.5:p.Val284=
ENST00000635871.1:n.321C>A
ENST00000220420.9:c.852C>A	ENSP00000220420.5:p.Val284=
ENST00000349114.8:c.606C>A	ENSP00000220419.8:p.Val202=
ENST00000610827.4:c.849C>A	ENSP00000479732.1:p.Val283=
ENST00000611276.4:c.603C>A	ENSP00000482542.1:p.Val201=
ENST00000622115.1:c.855C>A	ENSP00000479638.1:p.Val285=
NM_004245.3:c.606C>A	NP_004236.1:p.Val202=
NM_201631.3:c.852C>A	NP_963925.2:p.Val284=
XM_011522229.1:c.852C>A	XP_011520531.1:p.Val284=
XR_931948.1:n.1026C>A
NM_004245.4:c.606C>A	NP_004236.1:p.Val202=
NM_201631.4:c.852C>A MANE Select	NP_963925.2:p.Val284=