Canonical Allele Identifier: CA913189333

Linked Data

ClinVar Variation Id: 623273
ClinVar RCV Id: RCV000761398

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109607813_109609831del , CM000663.2:g.109607813_109609831del GRCh38
NC_000001.10:g.110150435_110152453del , CM000663.1:g.110150435_110152453del GRCh37
NC_000001.9:g.109951958_109953976del NCBI36
NG_009099.1:g.8409_10427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000351050.8:c.303+365_461+974del (GNAT2)
ENST00000679935.1:c.303+365_461+974del (GNAT2)
ENST00000351050.7:c.303+365_461+974del (GNAT2)
ENST00000369851.5:c.*15491_*17509del (GNAI3) ENSP00000358867.4:n.*15491_*17509del
NM_005272.3:c.303+365_461+974del (GNAT2)
XM_011541264.1:c.303+365_461+974del (GNAT2)
XM_011541265.1:c.303+365_461+974del (GNAT2)
XM_011541266.1:c.303+365_461+974del (GNAT2)
XM_011541264.2:c.303+365_461+974del (GNAT2)
NM_001377295.1:c.303+365_461+974del (GNAT2)
NM_005272.5:c.303+365_461+974del (GNAT2)
NM_001377295.2:c.303+365_461+974del (GNAT2)
NM_001379232.1:c.303+365_461+974del (GNAT2)