Canonical Allele Identifier: CA2675343884

Gene: TXNDC15

Linked Data

• gnomAD v4: 5-134893480-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893480C>G , CM000667.2:g.134893480C>G	GRCh38
NC_000005.9:g.134229170C>G , CM000667.1:g.134229170C>G	GRCh37
NC_000005.8:g.134257069C>G	NCBI36
NG_053174.1:g.24711C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-12C>G MANE Select	ENSP00000351157.5:n.592-12C>G
ENST00000358387.8:c.592-12C>G	ENSP00000351157.4:n.592-12C>G
ENST00000505174.1:n.1303C>G
ENST00000506350.1:n.31-12C>G
ENST00000507024.5:c.*410-12C>G	ENSP00000424716.1:n.*410-12C>G
ENST00000508779.1:c.543-12C>G
ENST00000511070.5:c.104-12C>G	ENSP00000423609.1:n.104-12C>G
NM_024715.3:c.592-12C>G	NP_078991.3:n.592-12C>G
NM_001350735.1:c.388-12C>G	NP_001337664.1:n.388-12C>G
NM_024715.4:c.592-12C>G MANE Select	NP_078991.3:n.592-12C>G
NM_001350735.2:c.388-12C>G	NP_001337664.1:n.388-12C>G