Canonical Allele Identifier: CA361459236

Gene: TXNDC15

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.593A>C MANE Select	ENSP00000351157.5:p.Asp198Ala
ENST00000358387.8:c.593A>C	ENSP00000351157.4:p.Asp198Ala
ENST00000505174.1:n.1316A>C
ENST00000506350.1:n.32A>C
ENST00000507024.5:c.*411A>C	ENSP00000424716.1:n.*411A>C
ENST00000508779.1:c.544A>C
ENST00000511070.5:c.105A>C	ENSP00000423609.1:p.Gly35=
NM_024715.3:c.593A>C	NP_078991.3:p.Asp198Ala
NM_001350735.1:c.389A>C	NP_001337664.1:p.Asp130Ala
NM_024715.4:c.593A>C MANE Select	NP_078991.3:p.Asp198Ala
NM_001350735.2:c.389A>C	NP_001337664.1:p.Asp130Ala