Canonical Allele Identifier: CA361459240

Gene: TXNDC15

Linked Data

• MyVariant Identifiers: chr5:g.134229183A>T (hg19) ; chr5:g.134893493A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893493A>T , CM000667.2:g.134893493A>T	GRCh38
NC_000005.9:g.134229183A>T , CM000667.1:g.134229183A>T	GRCh37
NC_000005.8:g.134257082A>T	NCBI36
NG_053174.1:g.24724A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.593A>T MANE Select	ENSP00000351157.5:p.Asp198Val
ENST00000358387.8:c.593A>T	ENSP00000351157.4:p.Asp198Val
ENST00000505174.1:n.1316A>T
ENST00000506350.1:n.32A>T
ENST00000507024.5:c.*411A>T	ENSP00000424716.1:n.*411A>T
ENST00000508779.1:c.544A>T
ENST00000511070.5:c.105A>T	ENSP00000423609.1:p.Gly35=
NM_024715.3:c.593A>T	NP_078991.3:p.Asp198Val
NM_001350735.1:c.389A>T	NP_001337664.1:p.Asp130Val
NM_024715.4:c.593A>T MANE Select	NP_078991.3:p.Asp198Val
NM_001350735.2:c.389A>T	NP_001337664.1:p.Asp130Val