Canonical Allele Identifier: CA806475366

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1306316287
• MyVariant Identifiers: chr5:g.159367203_159367207del (hg19) ; chr5:g.159940196_159940200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940199_159940203del , CM000667.2:g.159940199_159940203del	GRCh38
NC_000005.9:g.159367206_159367210del , CM000667.1:g.159367206_159367210del	GRCh37
NC_000005.8:g.159299784_159299788del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+22345_949+22349del MANE Select	ENSP00000306662.3:n.949+22345_949+22349del
ENST00000306675.3:c.949+22345_949+22349del	ENSP00000306662.3:n.949+22345_949+22349del
NM_000679.3:c.949+22345_949+22349del	NP_000670.1:n.949+22345_949+22349del
XM_005265818.2:c.950-7491_950-7487del	XP_005265875.1:n.950-7491_950-7487del
XM_005265819.2:c.950-14914_950-14910del	XP_005265876.1:n.950-14914_950-14910del
XM_006714821.2:c.949+22345_949+22349del	XP_006714884.1:n.949+22345_949+22349del
XM_011534435.1:c.1057+14603_1057+14607del	XP_011532737.1:n.1057+14603_1057+14607del
XM_011534436.1:c.1057+14603_1057+14607del	XP_011532738.1:n.1057+14603_1057+14607del
XM_011534437.1:c.1058-7491_1058-7487del	XP_011532739.1:n.1058-7491_1058-7487del
XM_011534439.1:c.1057+14603_1057+14607del	XP_011532741.1:n.1057+14603_1057+14607del
XM_005265818.3:c.950-7491_950-7487del	XP_005265875.1:n.950-7491_950-7487del
XM_006714821.3:c.949+22345_949+22349del	XP_006714884.1:n.949+22345_949+22349del
XM_011534437.2:c.1058-7491_1058-7487del	XP_011532739.1:n.1058-7491_1058-7487del
XR_001742950.1:n.1418_1422del
NM_000679.4:c.949+22345_949+22349del MANE Select	NP_000670.1:n.949+22345_949+22349del