Canonical Allele Identifier: CA806475697

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1213522383
• gnomAD v3: 5-159940949-A-ACG
• gnomAD v4: 5-159940949-A-ACG
• MyVariant Identifiers: chr5:g.159367956_159367957insCG (hg19) ; chr5:g.159940949_159940950insCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159940950_159940951insGC , CM000667.2:g.159940950_159940951insGC	GRCh38
NC_000005.9:g.159367957_159367958insGC , CM000667.1:g.159367957_159367958insGC	GRCh37
NC_000005.8:g.159300535_159300536insGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+23096_949+23097insGC MANE Select	ENSP00000306662.3:n.949+23096_949+23097insGC
ENST00000306675.3:c.949+23096_949+23097insGC	ENSP00000306662.3:n.949+23096_949+23097insGC
NM_000679.3:c.949+23096_949+23097insGC	NP_000670.1:n.949+23096_949+23097insGC
XM_005265818.2:c.950-6740_950-6739insGC	XP_005265875.1:n.950-6740_950-6739insGC
XM_005265819.2:c.950-14163_950-14162insGC	XP_005265876.1:n.950-14163_950-14162insGC
XM_006714821.2:c.949+23096_949+23097insGC	XP_006714884.1:n.949+23096_949+23097insGC
XM_011534435.1:c.1057+15354_1057+15355insGC	XP_011532737.1:n.1057+15354_1057+15355insGC
XM_011534436.1:c.1058-14150_1058-14149insGC	XP_011532738.1:n.1058-14150_1058-14149insGC
XM_011534437.1:c.1058-6740_1058-6739insGC	XP_011532739.1:n.1058-6740_1058-6739insGC
XM_011534439.1:c.1058-14163_1058-14162insGC	XP_011532741.1:n.1058-14163_1058-14162insGC
XM_005265818.3:c.950-6740_950-6739insGC	XP_005265875.1:n.950-6740_950-6739insGC
XM_006714821.3:c.949+23096_949+23097insGC	XP_006714884.1:n.949+23096_949+23097insGC
XM_011534437.2:c.1058-6740_1058-6739insGC	XP_011532739.1:n.1058-6740_1058-6739insGC
XR_001742950.1:n.668_669insCG
NM_000679.4:c.949+23096_949+23097insGC MANE Select	NP_000670.1:n.949+23096_949+23097insGC