Canonical Allele Identifier: CA564102407
Gene: ADRA1B HGNC NCBI

Linked Data

dbSNP Id: rs1440493556

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159940912_159940913del , CM000667.2:g.159940912_159940913del GRCh38
NC_000005.9:g.159367919_159367920del , CM000667.1:g.159367919_159367920del GRCh37
NC_000005.8:g.159300497_159300498del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306675.5:c.949+23058_949+23059del MANE Select ENSP00000306662.3:n.949+23058_949+23059del
ENST00000306675.3:c.949+23058_949+23059del ENSP00000306662.3:n.949+23058_949+23059del
NM_000679.3:c.949+23058_949+23059del NP_000670.1:n.949+23058_949+23059del
XM_005265818.2:c.950-6778_950-6777del XP_005265875.1:n.950-6778_950-6777del
XM_005265819.2:c.950-14201_950-14200del XP_005265876.1:n.950-14201_950-14200del
XM_006714821.2:c.949+23058_949+23059del XP_006714884.1:n.949+23058_949+23059del
XM_011534435.1:c.1057+15316_1057+15317del XP_011532737.1:n.1057+15316_1057+15317del
XM_011534436.1:c.1058-14188_1058-14187del XP_011532738.1:n.1058-14188_1058-14187del
XM_011534437.1:c.1058-6778_1058-6777del XP_011532739.1:n.1058-6778_1058-6777del
XM_011534439.1:c.1058-14201_1058-14200del XP_011532741.1:n.1058-14201_1058-14200del
XM_005265818.3:c.950-6778_950-6777del XP_005265875.1:n.950-6778_950-6777del
XM_006714821.3:c.949+23058_949+23059del XP_006714884.1:n.949+23058_949+23059del
XM_011534437.2:c.1058-6778_1058-6777del XP_011532739.1:n.1058-6778_1058-6777del
XR_001742950.1:n.707_708del
NM_000679.4:c.949+23058_949+23059del MANE Select NP_000670.1:n.949+23058_949+23059del