Canonical Allele Identifier: CA3416887

Gene: TXNDC15

Linked Data

• dbSNP Id: rs754540351
• ExAC: 5:134229175 A / G
• gnomAD v2: 5-134229175-A-G
• gnomAD v4: 5-134893485-A-G
• MyVariant Identifiers: chr5:g.134229175A>G (hg19) ; chr5:g.134893485A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893485A>G , CM000667.2:g.134893485A>G	GRCh38
NC_000005.9:g.134229175A>G , CM000667.1:g.134229175A>G	GRCh37
NC_000005.8:g.134257074A>G	NCBI36
NG_053174.1:g.24716A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-7A>G MANE Select	ENSP00000351157.5:n.592-7A>G
ENST00000358387.8:c.592-7A>G	ENSP00000351157.4:n.592-7A>G
ENST00000505174.1:n.1308A>G
ENST00000506350.1:n.31-7A>G
ENST00000507024.5:c.*410-7A>G	ENSP00000424716.1:n.*410-7A>G
ENST00000508779.1:c.543-7A>G
ENST00000511070.5:c.104-7A>G	ENSP00000423609.1:n.104-7A>G
NM_024715.3:c.592-7A>G	NP_078991.3:n.592-7A>G
NM_001350735.1:c.388-7A>G	NP_001337664.1:n.388-7A>G
NM_024715.4:c.592-7A>G MANE Select	NP_078991.3:n.592-7A>G
NM_001350735.2:c.388-7A>G	NP_001337664.1:n.388-7A>G