Canonical Allele Identifier: CA1595294889
Gene: ADRA1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159920503_159920506delinsCCTT , CM000667.2:g.159920503_159920506delinsCCTT GRCh38
NC_000005.9:g.159347510_159347513delinsCCTT , CM000667.1:g.159347510_159347513delinsCCTT GRCh37
NC_000005.8:g.159280088_159280091delinsCCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306675.5:c.949+2649_949+2652delinsCCTT MANE Select ENSP00000306662.3:n.949+2649_949+2652deli...
ENST00000306675.3:c.949+2649_949+2652delinsCCTT ENSP00000306662.3:n.949+2649_949+2652deli...
NM_000679.3:c.949+2649_949+2652delinsCCTT NP_000670.1:n.949+2649_949+2652delinsCCTT...
XM_005265818.2:c.949+2649_949+2652delinsCCTT XP_005265875.1:n.949+2649_949+2652delinsC...
XM_005265819.2:c.949+2649_949+2652delinsCCTT XP_005265876.1:n.949+2649_949+2652delinsC...
XM_006714821.2:c.949+2649_949+2652delinsCCTT XP_006714884.1:n.949+2649_949+2652delinsC...
XM_011534435.1:c.949+2649_949+2652delinsCCTT XP_011532737.1:n.949+2649_949+2652delinsC...
XM_011534436.1:c.949+2649_949+2652delinsCCTT XP_011532738.1:n.949+2649_949+2652delinsC...
XM_011534437.1:c.949+2649_949+2652delinsCCTT XP_011532739.1:n.949+2649_949+2652delinsC...
XM_011534438.1:c.949+2649_949+2652delinsCCTT XP_011532740.1:n.949+2649_949+2652delinsC...
XM_011534439.1:c.949+2649_949+2652delinsCCTT XP_011532741.1:n.949+2649_949+2652delinsC...
XM_011534440.1:c.949+2649_949+2652delinsCCTT XP_011532742.1:n.949+2649_949+2652delinsC...
XM_005265818.3:c.949+2649_949+2652delinsCCTT XP_005265875.1:n.949+2649_949+2652delinsC...
XM_006714821.3:c.949+2649_949+2652delinsCCTT XP_006714884.1:n.949+2649_949+2652delinsC...
XM_011534437.2:c.949+2649_949+2652delinsCCTT XP_011532739.1:n.949+2649_949+2652delinsC...
XM_011534438.2:c.949+2649_949+2652delinsCCTT XP_011532740.1:n.949+2649_949+2652delinsC...
NM_000679.4:c.949+2649_949+2652delinsCCTT MANE Select NP_000670.1:n.949+2649_949+2652delinsCCTT...