Canonical Allele Identifier: CA1584260166

Gene: TXNDC15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893473_134893477delinsCTTGT , CM000667.2:g.134893473_134893477delinsCTTGT	GRCh38
NC_000005.9:g.134229163_134229167delinsCTTGT , CM000667.1:g.134229163_134229167delinsCTTGT	GRCh37
NC_000005.8:g.134257062_134257066delinsCTTGT	NCBI36
NG_053174.1:g.24704_24708delinsCTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-19_592-15delinsCTTGT MANE Select	ENSP00000351157.5:n.592-19_592-15delinsCTTGT
ENST00000358387.8:c.592-19_592-15delinsCTTGT	ENSP00000351157.4:n.592-19_592-15delinsCTTGT
ENST00000505174.1:n.1296_1300delinsCTTGT
ENST00000506350.1:n.31-19_31-15delinsCTTGT
ENST00000507024.5:c.*410-19_*410-15delinsCTTGT	ENSP00000424716.1:n.*410-19_*410-15delinsCTTGT
ENST00000508779.1:c.543-19_543-15delinsCTTGT
ENST00000511070.5:c.104-19_104-15delinsCTTGT	ENSP00000423609.1:n.104-19_104-15delinsCTTGT
NM_024715.3:c.592-19_592-15delinsCTTGT	NP_078991.3:n.592-19_592-15delinsCTTGT
NM_001350735.1:c.388-19_388-15delinsCTTGT	NP_001337664.1:n.388-19_388-15delinsCTTGT
NM_024715.4:c.592-19_592-15delinsCTTGT MANE Select	NP_078991.3:n.592-19_592-15delinsCTTGT
NM_001350735.2:c.388-19_388-15delinsCTTGT	NP_001337664.1:n.388-19_388-15delinsCTTGT