Canonical Allele Identifier: CA128384242
Gene: TXNDC15 HGNC NCBI

Linked Data

dbSNP Id: rs941152874

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134893488A>G , CM000667.2:g.134893488A>G GRCh38
NC_000005.9:g.134229178A>G , CM000667.1:g.134229178A>G GRCh37
NC_000005.8:g.134257077A>G NCBI36
NG_053174.1:g.24719A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358387.9:c.592-4A>G MANE Select ENSP00000351157.5:n.592-4A>G
ENST00000358387.8:c.592-4A>G ENSP00000351157.4:n.592-4A>G
ENST00000505174.1:n.1311A>G
ENST00000506350.1:n.31-4A>G
ENST00000507024.5:c.*410-4A>G ENSP00000424716.1:n.*410-4A>G
ENST00000508779.1:c.543-4A>G
ENST00000511070.5:c.104-4A>G ENSP00000423609.1:n.104-4A>G
NM_024715.3:c.592-4A>G NP_078991.3:n.592-4A>G
NM_001350735.1:c.388-4A>G NP_001337664.1:n.388-4A>G
NM_024715.4:c.592-4A>G MANE Select NP_078991.3:n.592-4A>G
NM_001350735.2:c.388-4A>G NP_001337664.1:n.388-4A>G