Canonical Allele Identifier: CA1261766037
Gene: TACR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.75186888G= , CM000664.2:g.75186888G= GRCh38
NC_000002.11:g.75414014G= , CM000664.1:g.75414014G= GRCh37
NC_000002.10:g.75267522G= NCBI36
NG_029522.1:g.17632C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305249.10:c.389+11658C= MANE Select ENSP00000303522.4:n.389+11658C=
ENST00000305249.9:c.389+11658C= ENSP00000303522.4:n.389+11658C=
ENST00000409848.3:c.389+11658C= ENSP00000386448.3:n.389+11658C=
NM_001058.3:c.389+11658C= NP_001049.1:n.389+11658C=
NM_015727.2:c.389+11658C= NP_056542.1:n.389+11658C=
XR_940257.1:n.108+40428G=
XR_940258.1:n.2432G=
XR_940259.1:n.353G=
XR_940257.2:n.109+40428G=
XR_940258.2:n.157G=
NM_001058.4:c.389+11658C= MANE Select NP_001049.1:n.389+11658C=
NM_015727.3:c.389+11658C= NP_056542.1:n.389+11658C=
NR_168009.1:n.372+30573G=
NR_168010.1:n.366+30573G=
NR_168011.1:n.425G=