Canonical Allele Identifier: CA392100040

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545125T>C (hg19) ; chr15:g.43252927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252927T>C , CM000677.2:g.43252927T>C	GRCh38
NC_000015.9:g.43545125T>C , CM000677.1:g.43545125T>C	GRCh37
NC_000015.8:g.41332417T>C	NCBI36
NG_016124.1:g.18931A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.694A>G MANE Select	ENSP00000220420.5:p.Asn232Asp
ENST00000635871.1:n.163A>G
ENST00000220420.9:c.694A>G	ENSP00000220420.5:p.Asn232Asp
ENST00000349114.8:c.448A>G	ENSP00000220419.8:p.Asn150Asp
ENST00000610827.4:c.691A>G	ENSP00000479732.1:p.Asn231Asp
ENST00000611276.4:c.445A>G	ENSP00000482542.1:p.Asn149Asp
ENST00000622115.1:c.697A>G	ENSP00000479638.1:p.Asn233Asp
NM_004245.3:c.448A>G	NP_004236.1:p.Asn150Asp
NM_201631.3:c.694A>G	NP_963925.2:p.Asn232Asp
XM_011522229.1:c.694A>G	XP_011520531.1:p.Asn232Asp
XR_931948.1:n.868A>G
NM_004245.4:c.448A>G	NP_004236.1:p.Asn150Asp
NM_201631.4:c.694A>G MANE Select	NP_963925.2:p.Asn232Asp