Canonical Allele Identifier: CA490131432

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43544958T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252760T>A , CM000677.2:g.43252760T>A	GRCh38
NC_000015.9:g.43544958T>A , CM000677.1:g.43544958T>A	GRCh37
NC_000015.8:g.41332250T>A	NCBI36
NG_016124.1:g.19098A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220420.10:c.861A>T MANE Select	ENSP00000220420.5:p.Thr287=
ENST00000635871.1:n.330A>T
ENST00000220420.9:c.861A>T	ENSP00000220420.5:p.Thr287=
ENST00000349114.8:c.615A>T	ENSP00000220419.8:p.Thr205=
ENST00000610827.4:c.858A>T	ENSP00000479732.1:p.Thr286=
ENST00000611276.4:c.612A>T	ENSP00000482542.1:p.Thr204=
ENST00000622115.1:c.864A>T	ENSP00000479638.1:p.Thr288=
NM_004245.3:c.615A>T	NP_004236.1:p.Thr205=
NM_201631.3:c.861A>T	NP_963925.2:p.Thr287=
XM_011522229.1:c.861A>T	XP_011520531.1:p.Thr287=
XR_931948.1:n.1035A>T
NM_004245.4:c.615A>T	NP_004236.1:p.Thr205=
NM_201631.4:c.861A>T MANE Select	NP_963925.2:p.Thr287=