Canonical Allele Identifier: CA392100673

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545735G>C (hg19) ; chr15:g.43253537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43253537G>C , CM000677.2:g.43253537G>C	GRCh38
NC_000015.9:g.43545735G>C , CM000677.1:g.43545735G>C	GRCh37
NC_000015.8:g.41333027G>C	NCBI36
NG_016124.1:g.18321C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.653C>G MANE Select	ENSP00000220420.5:p.Pro218Arg
ENST00000635871.1:n.122C>G
ENST00000220420.9:c.653C>G	ENSP00000220420.5:p.Pro218Arg
ENST00000349114.8:c.407C>G	ENSP00000220419.8:p.Pro136Arg
ENST00000610827.4:c.650C>G	ENSP00000479732.1:p.Pro217Arg
ENST00000611276.4:c.404C>G	ENSP00000482542.1:p.Pro135Arg
ENST00000622115.1:c.656C>G	ENSP00000479638.1:p.Pro219Arg
NM_004245.3:c.407C>G	NP_004236.1:p.Pro136Arg
NM_201631.3:c.653C>G	NP_963925.2:p.Pro218Arg
XM_011522229.1:c.653C>G	XP_011520531.1:p.Pro218Arg
XR_931948.1:n.827C>G
NM_004245.4:c.407C>G	NP_004236.1:p.Pro136Arg
NM_201631.4:c.653C>G MANE Select	NP_963925.2:p.Pro218Arg