Canonical Allele Identifier: CA130820213

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1023235886
• gnomAD v2: 5-159364823-CAG-C
• MyVariant Identifiers: chr5:g.159364824_159364825del (hg19) ; chr5:g.159937817_159937818del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159937818_159937819del , CM000667.2:g.159937818_159937819del	GRCh38
NC_000005.9:g.159364825_159364826del , CM000667.1:g.159364825_159364826del	GRCh37
NC_000005.8:g.159297403_159297404del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+19964_949+19965del MANE Select	ENSP00000306662.3:n.949+19964_949+19965del
ENST00000306675.3:c.949+19964_949+19965del	ENSP00000306662.3:n.949+19964_949+19965del
NM_000679.3:c.949+19964_949+19965del	NP_000670.1:n.949+19964_949+19965del
XM_005265818.2:c.950-9872_950-9871del	XP_005265875.1:n.950-9872_950-9871del
XM_005265819.2:c.950-17295_950-17294del	XP_005265876.1:n.950-17295_950-17294del
XM_006714821.2:c.949+19964_949+19965del	XP_006714884.1:n.949+19964_949+19965del
XM_011534435.1:c.1057+12222_1057+12223del	XP_011532737.1:n.1057+12222_1057+12223del
XM_011534436.1:c.1057+12222_1057+12223del	XP_011532738.1:n.1057+12222_1057+12223del
XM_011534437.1:c.1058-9872_1058-9871del	XP_011532739.1:n.1058-9872_1058-9871del
XM_011534439.1:c.1057+12222_1057+12223del	XP_011532741.1:n.1057+12222_1057+12223del
XM_005265818.3:c.950-9872_950-9871del	XP_005265875.1:n.950-9872_950-9871del
XM_006714821.3:c.949+19964_949+19965del	XP_006714884.1:n.949+19964_949+19965del
XM_011534437.2:c.1058-9872_1058-9871del	XP_011532739.1:n.1058-9872_1058-9871del
XR_001742950.1:n.3800_3801del
NM_000679.4:c.949+19964_949+19965del MANE Select	NP_000670.1:n.949+19964_949+19965del