Canonical Allele Identifier: CA919551183
Gene: GABPB1 HGNC NCBI

Linked Data

dbSNP Id: rs1555513647

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50329532_50329533insTTTT , CM000677.2:g.50329532_50329533insTTTT GRCh38
NC_000015.9:g.50621729_50621730insTTTT , CM000677.1:g.50621729_50621730insTTTT GRCh37
NC_000015.8:g.48409021_48409022insTTTT NCBI36
NG_029475.1:g.30878_30879insAAAA
NG_029475.2:g.30878_30879insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380877.8:c.1-19733_1-19732insAAAA MANE Select ENSP00000370259.3:n.1-19733_1-19732insAAAA
ENST00000220429.12:c.1-19733_1-19732insAAAA ENSP00000220429.8:n.1-19733_1-19732insAAAA
ENST00000359031.8:c.-1+16841_-1+16842insAAAA ENSP00000351923.4:n.-1+16841_-1+16842insAAAA
ENST00000380877.7:c.1-19733_1-19732insAAAA ENSP00000370259.3:n.1-19733_1-19732insAAAA
ENST00000396464.7:c.1-19733_1-19732insAAAA ENSP00000379728.3:n.1-19733_1-19732insAAAA
ENST00000429662.6:c.1-19733_1-19732insAAAA ENSP00000395771.2:n.1-19733_1-19732insAAAA
ENST00000543881.5:c.-120-25398_-120-25397insAAAA ENSP00000442500.1:n.-120-25398_-120-25397insAAAA
ENST00000558970.2:c.-255-14861_-255-14860insAAAA ENSP00000454211.1:n.-255-14861_-255-14860insAAAA
ENST00000560825.5:c.-1+16841_-1+16842insAAAA ENSP00000453463.1:n.-1+16841_-1+16842insAAAA
NM_002041.4:c.1-19733_1-19732insAAAA NP_002032.2:n.1-19733_1-19732insAAAA
NM_005254.5:c.1-19733_1-19732insAAAA NP_005245.2:n.1-19733_1-19732insAAAA
NM_016654.4:c.1-19733_1-19732insAAAA NP_057738.1:n.1-19733_1-19732insAAAA
NM_016655.4:c.1-19733_1-19732insAAAA NP_057739.1:n.1-19733_1-19732insAAAA
NM_181427.3:c.-1+16841_-1+16842insAAAA NP_852092.1:n.-1+16841_-1+16842insAAAA
XM_005254273.3:c.-1+16841_-1+16842insAAAA XP_005254330.1:n.-1+16841_-1+16842insAAAA
NM_001320910.1:c.-1+16841_-1+16842insAAAA NP_001307839.1:n.-1+16841_-1+16842insAAAA
NM_001320915.1:c.-1+16841_-1+16842insAAAA NP_001307844.1:n.-1+16841_-1+16842insAAAA
XM_011521426.3:c.1-19733_1-19732insAAAA XP_011519728.1:n.1-19733_1-19732insAAAA
XM_017022053.2:c.-1+16841_-1+16842insAAAA XP_016877542.1:n.-1+16841_-1+16842insAAAA
XM_017022054.2:c.-1+16841_-1+16842insAAAA XP_016877543.1:n.-1+16841_-1+16842insAAAA
XM_024449883.1:c.15+10972_15+10973insAAAA XP_024305651.1:n.15+10972_15+10973insAAAA
XM_024449884.1:c.15+10972_15+10973insAAAA XP_024305652.1:n.15+10972_15+10973insAAAA
XM_024449885.1:c.-60-2094_-60-2093insAAAA XP_024305653.1:n.-60-2094_-60-2093insAAAA
XM_024449886.1:c.1-19733_1-19732insAAAA XP_024305654.1:n.1-19733_1-19732insAAAA
XM_024449887.1:c.15+10972_15+10973insAAAA XP_024305655.1:n.15+10972_15+10973insAAAA
XM_024449888.1:c.15+10972_15+10973insAAAA XP_024305656.1:n.15+10972_15+10973insAAAA
NM_001320910.2:c.-1+16841_-1+16842insAAAA NP_001307839.1:n.-1+16841_-1+16842insAAAA
NM_001320915.2:c.-1+16841_-1+16842insAAAA NP_001307844.1:n.-1+16841_-1+16842insAAAA
NM_005254.6:c.1-19733_1-19732insAAAA NP_005245.2:n.1-19733_1-19732insAAAA
NM_016654.5:c.1-19733_1-19732insAAAA MANE Select NP_057738.1:n.1-19733_1-19732insAAAA
NM_002041.5:c.1-19733_1-19732insAAAA NP_002032.2:n.1-19733_1-19732insAAAA
NM_016655.5:c.1-19733_1-19732insAAAA NP_057739.1:n.1-19733_1-19732insAAAA
NM_181427.4:c.-1+16841_-1+16842insAAAA NP_852092.1:n.-1+16841_-1+16842insAAAA