Canonical Allele Identifier: CA361459230

Gene: TXNDC15

Linked Data

• MyVariant Identifiers: chr5:g.134229182G>C (hg19) ; chr5:g.134893492G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893492G>C , CM000667.2:g.134893492G>C	GRCh38
NC_000005.9:g.134229182G>C , CM000667.1:g.134229182G>C	GRCh37
NC_000005.8:g.134257081G>C	NCBI36
NG_053174.1:g.24723G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592G>C MANE Select	ENSP00000351157.5:p.Asp198His
ENST00000358387.8:c.592G>C	ENSP00000351157.4:p.Asp198His
ENST00000505174.1:n.1315G>C
ENST00000506350.1:n.31G>C
ENST00000507024.5:c.*410G>C	ENSP00000424716.1:n.*410G>C
ENST00000508779.1:c.543G>C
ENST00000511070.5:c.104G>C	ENSP00000423609.1:p.Gly35Ala
NM_024715.3:c.592G>C	NP_078991.3:p.Asp198His
NM_001350735.1:c.388G>C	NP_001337664.1:p.Asp130His
NM_024715.4:c.592G>C MANE Select	NP_078991.3:p.Asp198His
NM_001350735.2:c.388G>C	NP_001337664.1:p.Asp130His