Canonical Allele Identifier: CA361459247

Gene: TXNDC15

Linked Data

• MyVariant Identifiers: chr5:g.134229185C>A (hg19) ; chr5:g.134893495C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893495C>A , CM000667.2:g.134893495C>A	GRCh38
NC_000005.9:g.134229185C>A , CM000667.1:g.134229185C>A	GRCh37
NC_000005.8:g.134257084C>A	NCBI36
NG_053174.1:g.24726C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000358387.9:c.595C>A MANE Select	ENSP00000351157.5:p.Leu199Ile
ENST00000358387.8:c.595C>A	ENSP00000351157.4:p.Leu199Ile
ENST00000505174.1:n.1318C>A
ENST00000506350.1:n.34C>A
ENST00000507024.5:c.*413C>A	ENSP00000424716.1:n.*413C>A
ENST00000508779.1:c.546C>A
ENST00000511070.5:c.107C>A	ENSP00000423609.1:p.Pro36His
NM_024715.3:c.595C>A	NP_078991.3:p.Leu199Ile
NM_001350735.1:c.391C>A	NP_001337664.1:p.Leu131Ile
NM_024715.4:c.595C>A MANE Select	NP_078991.3:p.Leu199Ile
NM_001350735.2:c.391C>A	NP_001337664.1:p.Leu131Ile