Canonical Allele Identifier: CA2578411059

Gene: TXNDC15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893487C>T , CM000667.2:g.134893487C>T	GRCh38
NC_000005.9:g.134229177C>T , CM000667.1:g.134229177C>T	GRCh37
NC_000005.8:g.134257076C>T	NCBI36
NG_053174.1:g.24718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-5C>T MANE Select	ENSP00000351157.5:n.592-5C>T
ENST00000358387.8:c.592-5C>T	ENSP00000351157.4:n.592-5C>T
ENST00000505174.1:n.1310C>T
ENST00000506350.1:n.31-5C>T
ENST00000507024.5:c.*410-5C>T	ENSP00000424716.1:n.*410-5C>T
ENST00000508779.1:c.543-5C>T
ENST00000511070.5:c.104-5C>T	ENSP00000423609.1:n.104-5C>T
NM_024715.3:c.592-5C>T	NP_078991.3:n.592-5C>T
NM_001350735.1:c.388-5C>T	NP_001337664.1:n.388-5C>T
NM_024715.4:c.592-5C>T MANE Select	NP_078991.3:n.592-5C>T
NM_001350735.2:c.388-5C>T	NP_001337664.1:n.388-5C>T