Canonical Allele Identifier: CA15160043
Gene: TACR1 HGNC NCBI

Linked Data

dbSNP Id: rs3771856
gnomAD v2: 2-75414014-G-A
gnomAD v3: 2-75186888-G-A
gnomAD v4: 2-75186888-G-A

Genomic Alleles

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

Transcript Alleles

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