Canonical Allele Identifier: CA690248990

Gene: TAC3

Linked Data

• dbSNP Id: rs1376945887
• gnomAD v4: 12-57013300-A-G
• MyVariant Identifiers: chr12:g.57407084A>G (hg19) ; chr12:g.57013300A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57013300A>G , CM000674.2:g.57013300A>G	GRCh38
NC_000012.11:g.57407084A>G , CM000674.1:g.57407084A>G	GRCh37
NC_000012.10:g.55693351A>G	NCBI36
NG_021398.1:g.8261T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458521.7:c.238+59T>C MANE Select	ENSP00000404056.2:n.238+59T>C
ENST00000300108.7:c.238+59T>C	ENSP00000300108.3:n.238+59T>C
ENST00000357616.7:c.238+59T>C	ENSP00000350236.3:n.238+59T>C
ENST00000379411.6:c.238+59T>C	ENSP00000368721.2:n.238+59T>C
ENST00000393867.5:c.238+59T>C	ENSP00000377445.1:n.238+59T>C
ENST00000415231.1:c.238+59T>C	ENSP00000402995.1:n.238+59T>C
ENST00000423597.5:c.238+59T>C	ENSP00000416292.1:n.238+59T>C
ENST00000438756.5:c.238+59T>C	ENSP00000408131.1:n.238+59T>C
ENST00000441881.5:c.238+59T>C	ENSP00000408208.1:n.238+59T>C
ENST00000458521.6:c.238+59T>C	ENSP00000404056.2:n.238+59T>C
ENST00000496757.1:n.445T>C
ENST00000615887.4:c.238+59T>C	ENSP00000483110.1:n.238+59T>C
NM_001178054.1:c.238+59T>C	NP_001171525.1:n.238+59T>C
NM_013251.3:c.238+59T>C	NP_037383.1:n.238+59T>C
NR_033654.1:n.417+59T>C
XM_011538711.1:c.238+59T>C	XP_011537013.1:n.238+59T>C
NR_135164.1:n.417+59T>C
NR_135165.1:n.417+59T>C
NR_135166.1:n.417+59T>C
NM_013251.4:c.238+59T>C MANE Select	NP_037383.1:n.238+59T>C
NM_001178054.2:c.238+59T>C	NP_001171525.1:n.238+59T>C
NR_033654.2:n.386+59T>C
NR_135164.2:n.386+59T>C
NR_135165.2:n.386+59T>C
NR_135166.2:n.386+59T>C