Canonical Allele Identifier: CA1595317256
Gene: ADRA1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159941053_159941054delinsTC , CM000667.2:g.159941053_159941054delinsTC GRCh38
NC_000005.9:g.159368060_159368061delinsTC , CM000667.1:g.159368060_159368061delinsTC GRCh37
NC_000005.8:g.159300638_159300639delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+23199_949+23200delinsTC MANE Select ENSP00000306662.3:n.949+23199_949+23200delinsTC
ENST00000306675.3:c.949+23199_949+23200delinsTC ENSP00000306662.3:n.949+23199_949+23200delinsTC
NM_000679.3:c.949+23199_949+23200delinsTC NP_000670.1:n.949+23199_949+23200delinsTC
XM_005265818.2:c.950-6637_950-6636delinsTC XP_005265875.1:n.950-6637_950-6636delinsTC
XM_005265819.2:c.950-14060_950-14059delinsTC XP_005265876.1:n.950-14060_950-14059delinsTC
XM_006714821.2:c.949+23199_949+23200delinsTC XP_006714884.1:n.949+23199_949+23200delinsTC
XM_011534435.1:c.1057+15457_1057+15458delinsTC XP_011532737.1:n.1057+15457_1057+15458delinsTC
XM_011534436.1:c.1058-14047_1058-14046delinsTC XP_011532738.1:n.1058-14047_1058-14046delinsTC
XM_011534437.1:c.1058-6637_1058-6636delinsTC XP_011532739.1:n.1058-6637_1058-6636delinsTC
XM_011534439.1:c.1058-14060_1058-14059delinsTC XP_011532741.1:n.1058-14060_1058-14059delinsTC
XM_005265818.3:c.950-6637_950-6636delinsTC XP_005265875.1:n.950-6637_950-6636delinsTC
XM_006714821.3:c.949+23199_949+23200delinsTC XP_006714884.1:n.949+23199_949+23200delinsTC
XM_011534437.2:c.1058-6637_1058-6636delinsTC XP_011532739.1:n.1058-6637_1058-6636delinsTC
XR_001742950.1:n.564_565delinsGA
NM_000679.4:c.949+23199_949+23200delinsTC MANE Select NP_000670.1:n.949+23199_949+23200delinsTC