Canonical Allele Identifier: CA806466283

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1179574027
• gnomAD v3: 5-159924290-CGTGT-C
• gnomAD v4: 5-159924290-CGTGT-C
• MyVariant Identifiers: chr5:g.159351298_159351301del (hg19) ; chr5:g.159924291_159924294del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159924293_159924296del , CM000667.2:g.159924293_159924296del	GRCh38
NC_000005.9:g.159351300_159351303del , CM000667.1:g.159351300_159351303del	GRCh37
NC_000005.8:g.159283878_159283881del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+6439_949+6442del MANE Select	ENSP00000306662.3:n.949+6439_949+6442del
ENST00000306675.3:c.949+6439_949+6442del	ENSP00000306662.3:n.949+6439_949+6442del
NM_000679.3:c.949+6439_949+6442del	NP_000670.1:n.949+6439_949+6442del
XM_005265818.2:c.949+6439_949+6442del	XP_005265875.1:n.949+6439_949+6442del
XM_005265819.2:c.949+6439_949+6442del	XP_005265876.1:n.949+6439_949+6442del
XM_006714821.2:c.949+6439_949+6442del	XP_006714884.1:n.949+6439_949+6442del
XM_011534435.1:c.950-1196_950-1193del	XP_011532737.1:n.950-1196_950-1193del
XM_011534436.1:c.950-1196_950-1193del	XP_011532738.1:n.950-1196_950-1193del
XM_011534437.1:c.950-1196_950-1193del	XP_011532739.1:n.950-1196_950-1193del
XM_011534438.1:c.950-1196_950-1193del	XP_011532740.1:n.950-1196_950-1193del
XM_011534439.1:c.950-1196_950-1193del	XP_011532741.1:n.950-1196_950-1193del
XM_011534440.1:c.950-1196_950-1193del	XP_011532742.1:n.950-1196_950-1193del
XM_005265818.3:c.949+6439_949+6442del	XP_005265875.1:n.949+6439_949+6442del
XM_006714821.3:c.949+6439_949+6442del	XP_006714884.1:n.949+6439_949+6442del
XM_011534437.2:c.950-1196_950-1193del	XP_011532739.1:n.950-1196_950-1193del
XM_011534438.2:c.950-1196_950-1193del	XP_011532740.1:n.950-1196_950-1193del
NM_000679.4:c.949+6439_949+6442del MANE Select	NP_000670.1:n.949+6439_949+6442del