Canonical Allele Identifier: CA1584260169
Gene: TXNDC15 HGNC NCBI

Linked Data

dbSNP Id: rs1750427144

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134893474T>C , CM000667.2:g.134893474T>C GRCh38
NC_000005.9:g.134229164T>C , CM000667.1:g.134229164T>C GRCh37
NC_000005.8:g.134257063T>C NCBI36
NG_053174.1:g.24705T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358387.9:c.592-18T>C MANE Select ENSP00000351157.5:n.592-18T>C
ENST00000358387.8:c.592-18T>C ENSP00000351157.4:n.592-18T>C
ENST00000505174.1:n.1297T>C
ENST00000506350.1:n.31-18T>C
ENST00000507024.5:c.*410-18T>C ENSP00000424716.1:n.*410-18T>C
ENST00000508779.1:c.543-18T>C
ENST00000511070.5:c.104-18T>C ENSP00000423609.1:n.104-18T>C
NM_024715.3:c.592-18T>C NP_078991.3:n.592-18T>C
NM_001350735.1:c.388-18T>C NP_001337664.1:n.388-18T>C
NM_024715.4:c.592-18T>C MANE Select NP_078991.3:n.592-18T>C
NM_001350735.2:c.388-18T>C NP_001337664.1:n.388-18T>C