Canonical Allele Identifier: CA392099774

Gene: TGM5

Linked Data

• MyVariant Identifiers: chr15:g.43545098T>G (hg19) ; chr15:g.43252900T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43252900T>G , CM000677.2:g.43252900T>G	GRCh38
NC_000015.9:g.43545098T>G , CM000677.1:g.43545098T>G	GRCh37
NC_000015.8:g.41332390T>G	NCBI36
NG_016124.1:g.18958A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220420.10:c.721A>C MANE Select	ENSP00000220420.5:p.Asn241His
ENST00000635871.1:n.190A>C
ENST00000220420.9:c.721A>C	ENSP00000220420.5:p.Asn241His
ENST00000349114.8:c.475A>C	ENSP00000220419.8:p.Asn159His
ENST00000610827.4:c.718A>C	ENSP00000479732.1:p.Asn240His
ENST00000611276.4:c.472A>C	ENSP00000482542.1:p.Asn158His
ENST00000622115.1:c.724A>C	ENSP00000479638.1:p.Asn242His
NM_004245.3:c.475A>C	NP_004236.1:p.Asn159His
NM_201631.3:c.721A>C	NP_963925.2:p.Asn241His
XM_011522229.1:c.721A>C	XP_011520531.1:p.Asn241His
XR_931948.1:n.895A>C
NM_004245.4:c.475A>C	NP_004236.1:p.Asn159His
NM_201631.4:c.721A>C MANE Select	NP_963925.2:p.Asn241His