Canonical Allele Identifier: CA361459243

Gene: TXNDC15

Linked Data

• gnomAD v4: 5-134893494-C-A
• MyVariant Identifiers: chr5:g.134229184C>A (hg19) ; chr5:g.134893494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893494C>A , CM000667.2:g.134893494C>A	GRCh38
NC_000005.9:g.134229184C>A , CM000667.1:g.134229184C>A	GRCh37
NC_000005.8:g.134257083C>A	NCBI36
NG_053174.1:g.24725C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358387.9:c.594C>A MANE Select	ENSP00000351157.5:p.Asp198Glu
ENST00000358387.8:c.594C>A	ENSP00000351157.4:p.Asp198Glu
ENST00000505174.1:n.1317C>A
ENST00000506350.1:n.33C>A
ENST00000507024.5:c.*412C>A	ENSP00000424716.1:n.*412C>A
ENST00000508779.1:c.545C>A
ENST00000511070.5:c.106C>A	ENSP00000423609.1:p.Pro36Thr
NM_024715.3:c.594C>A	NP_078991.3:p.Asp198Glu
NM_001350735.1:c.390C>A	NP_001337664.1:p.Asp130Glu
NM_024715.4:c.594C>A MANE Select	NP_078991.3:p.Asp198Glu
NM_001350735.2:c.390C>A	NP_001337664.1:p.Asp130Glu