Canonical Allele Identifier: CA1261768204
Gene: TACR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.75192588C= , CM000664.2:g.75192588C= GRCh38
NC_000002.11:g.75419714C= , CM000664.1:g.75419714C= GRCh37
NC_000002.10:g.75273222C= NCBI36
NG_029522.1:g.11932G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305249.10:c.389+5958G= MANE Select ENSP00000303522.4:n.389+5958G=
ENST00000305249.9:c.389+5958G= ENSP00000303522.4:n.389+5958G=
ENST00000409848.3:c.389+5958G= ENSP00000386448.3:n.389+5958G=
NM_001058.3:c.389+5958G= NP_001049.1:n.389+5958G=
NM_015727.2:c.389+5958G= NP_056542.1:n.389+5958G=
XR_940257.1:n.108+46128C=
XR_940257.2:n.109+46128C=
NM_001058.4:c.389+5958G= MANE Select NP_001049.1:n.389+5958G=
NM_015727.3:c.389+5958G= NP_056542.1:n.389+5958G=
NR_168009.1:n.372+36273C=
NR_168010.1:n.366+36273C=