Canonical Allele Identifier: CA2675343886

Gene: TXNDC15

Linked Data

• gnomAD v4: 5-134893489-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893489C>G , CM000667.2:g.134893489C>G	GRCh38
NC_000005.9:g.134229179C>G , CM000667.1:g.134229179C>G	GRCh37
NC_000005.8:g.134257078C>G	NCBI36
NG_053174.1:g.24720C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000358387.9:c.592-3C>G MANE Select	ENSP00000351157.5:n.592-3C>G
ENST00000358387.8:c.592-3C>G	ENSP00000351157.4:n.592-3C>G
ENST00000505174.1:n.1312C>G
ENST00000506350.1:n.31-3C>G
ENST00000507024.5:c.*410-3C>G	ENSP00000424716.1:n.*410-3C>G
ENST00000508779.1:c.543-3C>G
ENST00000511070.5:c.104-3C>G	ENSP00000423609.1:n.104-3C>G
NM_024715.3:c.592-3C>G	NP_078991.3:n.592-3C>G
NM_001350735.1:c.388-3C>G	NP_001337664.1:n.388-3C>G
NM_024715.4:c.592-3C>G MANE Select	NP_078991.3:n.592-3C>G
NM_001350735.2:c.388-3C>G	NP_001337664.1:n.388-3C>G