Canonical Allele Identifier: CA1595301926

Gene: ADRA1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159933552_159933553delinsAG , CM000667.2:g.159933552_159933553delinsAG	GRCh38
NC_000005.9:g.159360559_159360560delinsAG , CM000667.1:g.159360559_159360560delinsAG	GRCh37
NC_000005.8:g.159293137_159293138delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+15698_949+15699delinsAG MANE Select	ENSP00000306662.3:n.949+15698_949+15699delinsAG
ENST00000306675.3:c.949+15698_949+15699delinsAG	ENSP00000306662.3:n.949+15698_949+15699delinsAG
NM_000679.3:c.949+15698_949+15699delinsAG	NP_000670.1:n.949+15698_949+15699delinsAG
XM_005265818.2:c.950-14138_950-14137delinsAG	XP_005265875.1:n.950-14138_950-14137delinsAG
XM_005265819.2:c.949+15698_949+15699delinsAG	XP_005265876.1:n.949+15698_949+15699delinsAG
XM_006714821.2:c.949+15698_949+15699delinsAG	XP_006714884.1:n.949+15698_949+15699delinsAG
XM_011534435.1:c.1057+7956_1057+7957delinsAG	XP_011532737.1:n.1057+7956_1057+7957delinsAG
XM_011534436.1:c.1057+7956_1057+7957delinsAG	XP_011532738.1:n.1057+7956_1057+7957delinsAG
XM_011534437.1:c.1057+7956_1057+7957delinsAG	XP_011532739.1:n.1057+7956_1057+7957delinsAG
XM_011534439.1:c.1057+7956_1057+7957delinsAG	XP_011532741.1:n.1057+7956_1057+7957delinsAG
XM_005265818.3:c.950-14138_950-14137delinsAG	XP_005265875.1:n.950-14138_950-14137delinsAG
XM_006714821.3:c.949+15698_949+15699delinsAG	XP_006714884.1:n.949+15698_949+15699delinsAG
XM_011534437.2:c.1057+7956_1057+7957delinsAG	XP_011532739.1:n.1057+7956_1057+7957delinsAG
NM_000679.4:c.949+15698_949+15699delinsAG MANE Select	NP_000670.1:n.949+15698_949+15699delinsAG