Canonical Allele Identifier: CA563030969

Gene: TXNDC15

Linked Data

• dbSNP Id: rs1280713527
• gnomAD v2: 5-134229176-C-T
• gnomAD v4: 5-134893486-C-T
• MyVariant Identifiers: chr5:g.134229176C>T (hg19) ; chr5:g.134893486C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134893486C>T , CM000667.2:g.134893486C>T	GRCh38
NC_000005.9:g.134229176C>T , CM000667.1:g.134229176C>T	GRCh37
NC_000005.8:g.134257075C>T	NCBI36
NG_053174.1:g.24717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358387.9:c.592-6C>T MANE Select	ENSP00000351157.5:n.592-6C>T
ENST00000358387.8:c.592-6C>T	ENSP00000351157.4:n.592-6C>T
ENST00000505174.1:n.1309C>T
ENST00000506350.1:n.31-6C>T
ENST00000507024.5:c.*410-6C>T	ENSP00000424716.1:n.*410-6C>T
ENST00000508779.1:c.543-6C>T
ENST00000511070.5:c.104-6C>T	ENSP00000423609.1:n.104-6C>T
NM_024715.3:c.592-6C>T	NP_078991.3:n.592-6C>T
NM_001350735.1:c.388-6C>T	NP_001337664.1:n.388-6C>T
NM_024715.4:c.592-6C>T MANE Select	NP_078991.3:n.592-6C>T
NM_001350735.2:c.388-6C>T	NP_001337664.1:n.388-6C>T