Canonical Allele Identifier: CA1584260171

Gene: TXNDC15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893475T= , CM000667.2:g.134893475T=	GRCh38
NC_000005.9:g.134229165T= , CM000667.1:g.134229165T=	GRCh37
NC_000005.8:g.134257064T=	NCBI36
NG_053174.1:g.24706T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358387.9:c.592-17T= MANE Select	ENSP00000351157.5:n.592-17T=
ENST00000358387.8:c.592-17T=	ENSP00000351157.4:n.592-17T=
ENST00000505174.1:n.1298T=
ENST00000506350.1:n.31-17T=
ENST00000507024.5:c.*410-17T=	ENSP00000424716.1:n.*410-17T=
ENST00000508779.1:c.543-17T=
ENST00000511070.5:c.104-17T=	ENSP00000423609.1:n.104-17T=
NM_024715.3:c.592-17T=	NP_078991.3:n.592-17T=
NM_001350735.1:c.388-17T=	NP_001337664.1:n.388-17T=
NM_024715.4:c.592-17T= MANE Select	NP_078991.3:n.592-17T=
NM_001350735.2:c.388-17T=	NP_001337664.1:n.388-17T=