Canonical Allele Identifier: CA2137154936

Gene: TXNDC16

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52522510G>C , CM000676.2:g.52522510G>C	GRCh38
NC_000014.8:g.52989228G>C , CM000676.1:g.52989228G>C	GRCh37
NC_000014.7:g.52058978G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281741.9:c.393-3217C>G MANE Select	ENSP00000281741.4:n.393-3217C>G
ENST00000281741.8:c.393-3217C>G	ENSP00000281741.4:n.393-3217C>G
ENST00000554399.1:n.207+29806C>G
ENST00000557374.1:c.-295+29806C>G	ENSP00000450839.1:n.-295+29806C>G
NM_001160047.1:c.393-3232C>G	NP_001153519.1:n.393-3232C>G
NM_020784.2:c.393-3217C>G	NP_065835.2:n.393-3217C>G
XR_943497.1:n.822-3217C>G
XR_943498.1:n.822-3217C>G
XM_017021505.1:c.393-3217C>G	XP_016876994.1:n.393-3217C>G
XR_001750462.1:n.822-3217C>G
XR_001750463.1:n.822-3217C>G
XR_001750464.1:n.494-3217C>G
XR_001750465.1:n.494-3217C>G
XR_001750466.1:n.494-3217C>G
NM_020784.3:c.393-3217C>G MANE Select	NP_065835.2:n.393-3217C>G
NM_001160047.2:c.393-3232C>G	NP_001153519.1:n.393-3232C>G