Canonical Allele Identifier: CA1261751455
Gene: TACR1 HGNC NCBI

Linked Data

dbSNP Id: rs3755468

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.75155265T>G , CM000664.2:g.75155265T>G GRCh38
NC_000002.11:g.75382391T>G , CM000664.1:g.75382391T>G GRCh37
NC_000002.10:g.75235899T>G NCBI36
NG_029522.1:g.49255A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305249.10:c.390-34497A>C MANE Select ENSP00000303522.4:n.390-34497A>C
ENST00000305249.9:c.390-34497A>C ENSP00000303522.4:n.390-34497A>C
ENST00000409848.3:c.390-34497A>C ENSP00000386448.3:n.390-34497A>C
NM_001058.3:c.390-34497A>C NP_001049.1:n.390-34497A>C
NM_015727.2:c.390-34497A>C NP_056542.1:n.390-34497A>C
XR_940257.1:n.108+8805T>G
XR_940258.1:n.1323T>G
XR_940259.1:n.182+694T>G
XR_940257.2:n.109+8805T>G
NM_001058.4:c.390-34497A>C MANE Select NP_001049.1:n.390-34497A>C
NM_015727.3:c.390-34497A>C NP_056542.1:n.390-34497A>C
NR_168009.1:n.254+694T>G
NR_168010.1:n.254+694T>G
NR_168011.1:n.254+694T>G