Canonical Allele Identifier: CA392099691

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545091C>A (hg19) ; chr15:g.43252893C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252893C>A , CM000677.2:g.43252893C>A	GRCh38
NC_000015.9:g.43545091C>A , CM000677.1:g.43545091C>A	GRCh37
NC_000015.8:g.41332383C>A	NCBI36
NG_016124.1:g.18965G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.728G>T MANE Select	ENSP00000220420.5:p.Ser243Ile
ENST00000635871.1:n.197G>T
ENST00000220420.9:c.728G>T	ENSP00000220420.5:p.Ser243Ile
ENST00000349114.8:c.482G>T	ENSP00000220419.8:p.Ser161Ile
ENST00000610827.4:c.725G>T	ENSP00000479732.1:p.Ser242Ile
ENST00000611276.4:c.479G>T	ENSP00000482542.1:p.Ser160Ile
ENST00000622115.1:c.731G>T	ENSP00000479638.1:p.Ser244Ile
NM_004245.3:c.482G>T	NP_004236.1:p.Ser161Ile
NM_201631.3:c.728G>T	NP_963925.2:p.Ser243Ile
XM_011522229.1:c.728G>T	XP_011520531.1:p.Ser243Ile
XR_931948.1:n.902G>T
NM_004245.4:c.482G>T	NP_004236.1:p.Ser161Ile
NM_201631.4:c.728G>T MANE Select	NP_963925.2:p.Ser243Ile