Canonical Allele Identifier: CA392098906

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43544977A>G (hg19) ; chr15:g.43252779A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252779A>G , CM000677.2:g.43252779A>G	GRCh38
NC_000015.9:g.43544977A>G , CM000677.1:g.43544977A>G	GRCh37
NC_000015.8:g.41332269A>G	NCBI36
NG_016124.1:g.19079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.842T>C MANE Select	ENSP00000220420.5:p.Phe281Ser
ENST00000635871.1:n.311T>C
ENST00000220420.9:c.842T>C	ENSP00000220420.5:p.Phe281Ser
ENST00000349114.8:c.596T>C	ENSP00000220419.8:p.Phe199Ser
ENST00000610827.4:c.839T>C	ENSP00000479732.1:p.Phe280Ser
ENST00000611276.4:c.593T>C	ENSP00000482542.1:p.Phe198Ser
ENST00000622115.1:c.845T>C	ENSP00000479638.1:p.Phe282Ser
NM_004245.3:c.596T>C	NP_004236.1:p.Phe199Ser
NM_201631.3:c.842T>C	NP_963925.2:p.Phe281Ser
XM_011522229.1:c.842T>C	XP_011520531.1:p.Phe281Ser
XR_931948.1:n.1016T>C
NM_004245.4:c.596T>C	NP_004236.1:p.Phe199Ser
NM_201631.4:c.842T>C MANE Select	NP_963925.2:p.Phe281Ser