Canonical Allele Identifier: CA1149323180
Gene: GNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1804306_1804307delinsAT , CM000663.2:g.1804306_1804307delinsAT GRCh38
NC_000001.10:g.1735745_1735746delinsAT , CM000663.1:g.1735745_1735746delinsAT GRCh37
NC_000001.9:g.1725605_1725606delinsAT NCBI36
NG_047052.1:g.91811_91812delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000439272.7:c.391+112_391+113delinsAT ENSP00000399741.3:n.391+112_391+113delinsAT
ENST00000615252.5:c.130+112_130+113delinsAT ENSP00000483532.1:n.130+112_130+113delinsAT
ENST00000703692.1:c.430+112_430+113delinsAT ENSP00000515427.1:n.430+112_430+113delinsAT
ENST00000703693.1:c.430+112_430+113delinsAT ENSP00000515428.1:n.430+112_430+113delinsAT
ENST00000703694.1:c.430+112_430+113delinsAT ENSP00000515429.1:n.430+112_430+113delinsAT
ENST00000703695.1:c.430+112_430+113delinsAT ENSP00000515430.1:n.430+112_430+113delinsAT
ENST00000703696.1:c.430+112_430+113delinsAT ENSP00000515431.1:n.430+112_430+113delinsAT
ENST00000703697.1:c.430+112_430+113delinsAT ENSP00000515432.1:n.430+112_430+113delinsAT
ENST00000703699.1:c.430+112_430+113delinsAT ENSP00000515433.1:n.430+112_430+113delinsAT
ENST00000703700.1:c.430+112_430+113delinsAT ENSP00000515434.1:n.430+112_430+113delinsAT
ENST00000703701.1:c.430+112_430+113delinsAT ENSP00000515435.1:n.430+112_430+113delinsAT
ENST00000703702.1:c.430+112_430+113delinsAT ENSP00000515436.1:n.430+112_430+113delinsAT
ENST00000703703.1:c.430+112_430+113delinsAT ENSP00000515437.1:n.430+112_430+113delinsAT
ENST00000703704.1:c.430+112_430+113delinsAT ENSP00000515438.1:n.430+112_430+113delinsAT
ENST00000703705.1:c.298+112_298+113delinsAT ENSP00000515439.1:n.298+112_298+113delinsAT
ENST00000703706.1:c.430+112_430+113delinsAT ENSP00000515440.1:n.430+112_430+113delinsAT
ENST00000703707.1:c.391+112_391+113delinsAT ENSP00000515441.1:n.391+112_391+113delinsAT
ENST00000703708.1:c.430+112_430+113delinsAT ENSP00000515442.1:n.430+112_430+113delinsAT
ENST00000703709.1:c.430+112_430+113delinsAT ENSP00000515443.1:n.430+112_430+113delinsAT
ENST00000703710.1:c.430+112_430+113delinsAT ENSP00000515444.1:n.430+112_430+113delinsAT
ENST00000703711.1:c.430+112_430+113delinsAT ENSP00000515445.1:n.430+112_430+113delinsAT
ENST00000378609.9:c.430+112_430+113delinsAT MANE Select ENSP00000367872.3:n.430+112_430+113delinsAT
ENST00000378609.8:c.430+112_430+113delinsAT ENSP00000367872.3:n.430+112_430+113delinsAT
ENST00000434686.6:c.430+112_430+113delinsAT ENSP00000392765.2:n.430+112_430+113delinsAT
ENST00000439272.6:c.391+112_391+113delinsAT ENSP00000399741.2:n.391+112_391+113delinsAT
ENST00000471354.1:n.1034+112_1034+113delinsAT
ENST00000610897.4:c.430+112_430+113delinsAT ENSP00000481878.1:n.430+112_430+113delinsAT
ENST00000615252.4:c.130+112_130+113delinsAT ENSP00000483532.1:n.130+112_130+113delinsAT
NM_001282538.1:c.130+112_130+113delinsAT NP_001269467.1:n.130+112_130+113delinsAT
NM_001282539.1:c.430+112_430+113delinsAT NP_001269468.1:n.430+112_430+113delinsAT
NM_002074.4:c.430+112_430+113delinsAT NP_002065.1:n.430+112_430+113delinsAT
XM_017001059.2:c.430+112_430+113delinsAT XP_016856548.1:n.430+112_430+113delinsAT
XM_017001060.2:c.430+112_430+113delinsAT XP_016856549.1:n.430+112_430+113delinsAT
XM_017001061.2:c.430+112_430+113delinsAT XP_016856550.1:n.430+112_430+113delinsAT
XM_024446495.1:c.430+112_430+113delinsAT XP_024302263.1:n.430+112_430+113delinsAT
NM_002074.5:c.430+112_430+113delinsAT MANE Select NP_002065.1:n.430+112_430+113delinsAT
NM_001282538.2:c.130+112_130+113delinsAT NP_001269467.1:n.130+112_130+113delinsAT
NM_001282539.2:c.430+112_430+113delinsAT NP_001269468.1:n.430+112_430+113delinsAT