Canonical Allele Identifier: CA2726246641

Gene: TAC3

Linked Data

• dbSNP Id: rs2136418921

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57013288C>G , CM000674.2:g.57013288C>G	GRCh38
NC_000012.11:g.57407072C>G , CM000674.1:g.57407072C>G	GRCh37
NC_000012.10:g.55693339C>G	NCBI36
NG_021398.1:g.8273G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000458521.7:c.238+71G>C MANE Select	ENSP00000404056.2:n.238+71G>C
ENST00000300108.7:c.238+71G>C	ENSP00000300108.3:n.238+71G>C
ENST00000357616.7:c.238+71G>C	ENSP00000350236.3:n.238+71G>C
ENST00000379411.6:c.238+71G>C	ENSP00000368721.2:n.238+71G>C
ENST00000393867.5:c.238+71G>C	ENSP00000377445.1:n.238+71G>C
ENST00000415231.1:c.238+71G>C	ENSP00000402995.1:n.238+71G>C
ENST00000423597.5:c.238+71G>C	ENSP00000416292.1:n.238+71G>C
ENST00000438756.5:c.238+71G>C	ENSP00000408131.1:n.238+71G>C
ENST00000441881.5:c.238+71G>C	ENSP00000408208.1:n.238+71G>C
ENST00000458521.6:c.238+71G>C	ENSP00000404056.2:n.238+71G>C
ENST00000496757.1:n.457G>C
ENST00000615887.4:c.238+71G>C	ENSP00000483110.1:n.238+71G>C
NM_001178054.1:c.238+71G>C	NP_001171525.1:n.238+71G>C
NM_013251.3:c.238+71G>C	NP_037383.1:n.238+71G>C
NR_033654.1:n.417+71G>C
XM_011538711.1:c.238+71G>C	XP_011537013.1:n.238+71G>C
NR_135164.1:n.417+71G>C
NR_135165.1:n.417+71G>C
NR_135166.1:n.417+71G>C
NM_013251.4:c.238+71G>C MANE Select	NP_037383.1:n.238+71G>C
NM_001178054.2:c.238+71G>C	NP_001171525.1:n.238+71G>C
NR_033654.2:n.386+71G>C
NR_135164.2:n.386+71G>C
NR_135165.2:n.386+71G>C
NR_135166.2:n.386+71G>C