Canonical Allele Identifier: CA185887

Gene: TAC3

Linked Data

• ClinVar Variation Id: 180155
• ClinVar RCV Id: RCV000156959 ; RCV000156960
• dbSNP Id: rs727505372
• MyVariant Identifiers: chr12:g.57407143G>T (hg19) ; chr12:g.57013359G>T (hg38)
• PubMed: PMID:25636053

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57013359G>T , CM000674.2:g.57013359G>T	GRCh38
NC_000012.11:g.57407143G>T , CM000674.1:g.57407143G>T	GRCh37
NC_000012.10:g.55693410G>T	NCBI36
NG_021398.1:g.8202C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458521.7:c.238C>A MANE Select	ENSP00000404056.2:p.Arg80Ser
ENST00000300108.7:c.238C>A	ENSP00000300108.3:p.Arg80Ser
ENST00000357616.7:c.238C>A	ENSP00000350236.3:p.Arg80Ser
ENST00000379411.6:c.238C>A	ENSP00000368721.2:p.His80Asn
ENST00000393867.5:c.238C>A	ENSP00000377445.1:p.Arg80Ser
ENST00000415231.1:c.238C>A	ENSP00000402995.1:p.Arg80Ser
ENST00000423597.5:c.238C>A	ENSP00000416292.1:p.His80Asn
ENST00000438756.5:c.238C>A	ENSP00000408131.1:p.Arg80Ser
ENST00000441881.5:c.238C>A	ENSP00000408208.1:p.His80Asn
ENST00000458521.6:c.238C>A	ENSP00000404056.2:p.Arg80Ser
ENST00000496757.1:n.386C>A
ENST00000615887.4:c.238C>A	ENSP00000483110.1:p.Arg80Ser
NM_001178054.1:c.238C>A	NP_001171525.1:p.His80Asn
NM_013251.3:c.238C>A	NP_037383.1:p.Arg80Ser
NR_033654.1:n.417C>A
XM_011538711.1:c.238C>A	XP_011537013.1:p.Arg80Ser
NR_135164.1:n.417C>A
NR_135165.1:n.417C>A
NR_135166.1:n.417C>A
NM_013251.4:c.238C>A MANE Select	NP_037383.1:p.Arg80Ser
NM_001178054.2:c.238C>A	NP_001171525.1:p.His80Asn
NR_033654.2:n.386C>A
NR_135164.2:n.386C>A
NR_135165.2:n.386C>A
NR_135166.2:n.386C>A