Canonical Allele Identifier: CA564102416

Gene: ADRA1B

Linked Data

• dbSNP Id: rs1336157006
• gnomAD v2: 5-159368060-TC-T
• gnomAD v3: 5-159941053-TC-T
• gnomAD v4: 5-159941053-TC-T
• MyVariant Identifiers: chr5:g.159368061del (hg19) ; chr5:g.159941054del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159941054del , CM000667.2:g.159941054del	GRCh38
NC_000005.9:g.159368061del , CM000667.1:g.159368061del	GRCh37
NC_000005.8:g.159300639del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000306675.5:c.949+23200del MANE Select	ENSP00000306662.3:n.949+23200del
ENST00000306675.3:c.949+23200del	ENSP00000306662.3:n.949+23200del
NM_000679.3:c.949+23200del	NP_000670.1:n.949+23200del
XM_005265818.2:c.950-6636del	XP_005265875.1:n.950-6636del
XM_005265819.2:c.950-14059del	XP_005265876.1:n.950-14059del
XM_006714821.2:c.949+23200del	XP_006714884.1:n.949+23200del
XM_011534435.1:c.1057+15458del	XP_011532737.1:n.1057+15458del
XM_011534436.1:c.1058-14046del	XP_011532738.1:n.1058-14046del
XM_011534437.1:c.1058-6636del	XP_011532739.1:n.1058-6636del
XM_011534439.1:c.1058-14059del	XP_011532741.1:n.1058-14059del
XM_005265818.3:c.950-6636del	XP_005265875.1:n.950-6636del
XM_006714821.3:c.949+23200del	XP_006714884.1:n.949+23200del
XM_011534437.2:c.1058-6636del	XP_011532739.1:n.1058-6636del
XR_001742950.1:n.564del
NM_000679.4:c.949+23200del MANE Select	NP_000670.1:n.949+23200del