Canonical Allele Identifier: CA2176348095
Gene: GABPB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.50318540_50318543delinsAAAG , CM000677.2:g.50318540_50318543delinsAAAG GRCh38
NC_000015.9:g.50610737_50610740delinsAAAG , CM000677.1:g.50610737_50610740delinsAAAG GRCh37
NC_000015.8:g.48398029_48398032delinsAAAG NCBI36
NG_029475.1:g.41866_41869delinsCTTT
NG_029475.2:g.41866_41869delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000380877.8:c.1-8745_1-8742delinsCTTT MANE Select ENSP00000370259.3:n.1-8745_1-8742delinsCT...
ENST00000220429.12:c.1-8745_1-8742delinsCTTT ENSP00000220429.8:n.1-8745_1-8742delinsCT...
ENST00000359031.8:c.1-8745_1-8742delinsCTTT ENSP00000351923.4:n.1-8745_1-8742delinsCT...
ENST00000380877.7:c.1-8745_1-8742delinsCTTT ENSP00000370259.3:n.1-8745_1-8742delinsCT...
ENST00000396464.7:c.1-8745_1-8742delinsCTTT ENSP00000379728.3:n.1-8745_1-8742delinsCT...
ENST00000429662.6:c.1-8745_1-8742delinsCTTT ENSP00000395771.2:n.1-8745_1-8742delinsCT...
ENST00000543881.5:c.-120-14410_-120-14407delinsCTTT ENSP00000442500.1:n.-120-14410_-120-14407...
ENST00000558335.5:c.-1+8650_-1+8653delinsCTTT ENSP00000453578.1:n.-1+8650_-1+8653delins...
ENST00000558970.2:c.-255-3873_-255-3870delinsCTTT ENSP00000454211.1:n.-255-3873_-255-3870de...
ENST00000560825.5:c.1-8745_1-8742delinsCTTT ENSP00000453463.1:n.1-8745_1-8742delinsCT...
NM_002041.4:c.1-8745_1-8742delinsCTTT NP_002032.2:n.1-8745_1-8742delinsCTTT
NM_005254.5:c.1-8745_1-8742delinsCTTT NP_005245.2:n.1-8745_1-8742delinsCTTT
NM_016654.4:c.1-8745_1-8742delinsCTTT NP_057738.1:n.1-8745_1-8742delinsCTTT
NM_016655.4:c.1-8745_1-8742delinsCTTT NP_057739.1:n.1-8745_1-8742delinsCTTT
NM_181427.3:c.1-8745_1-8742delinsCTTT NP_852092.1:n.1-8745_1-8742delinsCTTT
XM_005254273.3:c.1-8745_1-8742delinsCTTT XP_005254330.1:n.1-8745_1-8742delinsCTTT
XM_005254274.3:c.-1+8650_-1+8653delinsCTTT XP_005254331.1:n.-1+8650_-1+8653delinsCTT...
XM_011521427.1:c.-1+2859_-1+2862delinsCTTT XP_011519729.1:n.-1+2859_-1+2862delinsCTT...
NM_001320910.1:c.1-8745_1-8742delinsCTTT NP_001307839.1:n.1-8745_1-8742delinsCTTT
NM_001320915.1:c.1-8745_1-8742delinsCTTT NP_001307844.1:n.1-8745_1-8742delinsCTTT
XM_005254274.4:c.-1+8650_-1+8653delinsCTTT XP_005254331.1:n.-1+8650_-1+8653delinsCTT...
XM_011521426.3:c.1-8745_1-8742delinsCTTT XP_011519728.1:n.1-8745_1-8742delinsCTTT
XM_017022053.2:c.1-8745_1-8742delinsCTTT XP_016877542.1:n.1-8745_1-8742delinsCTTT
XM_017022054.2:c.1-8745_1-8742delinsCTTT XP_016877543.1:n.1-8745_1-8742delinsCTTT
XM_024449883.1:c.16-8745_16-8742delinsCTTT XP_024305651.1:n.16-8745_16-8742delinsCTT...
XM_024449884.1:c.16-8745_16-8742delinsCTTT XP_024305652.1:n.16-8745_16-8742delinsCTT...
XM_024449885.1:c.10-8745_10-8742delinsCTTT XP_024305653.1:n.10-8745_10-8742delinsCTT...
XM_024449886.1:c.1-8745_1-8742delinsCTTT XP_024305654.1:n.1-8745_1-8742delinsCTTT
XM_024449887.1:c.16-8745_16-8742delinsCTTT XP_024305655.1:n.16-8745_16-8742delinsCTT...
XM_024449888.1:c.16-8745_16-8742delinsCTTT XP_024305656.1:n.16-8745_16-8742delinsCTT...
NM_001320910.2:c.1-8745_1-8742delinsCTTT NP_001307839.1:n.1-8745_1-8742delinsCTTT
NM_001320915.2:c.1-8745_1-8742delinsCTTT NP_001307844.1:n.1-8745_1-8742delinsCTTT
NM_005254.6:c.1-8745_1-8742delinsCTTT NP_005245.2:n.1-8745_1-8742delinsCTTT
NM_016654.5:c.1-8745_1-8742delinsCTTT MANE Select NP_057738.1:n.1-8745_1-8742delinsCTTT
NM_002041.5:c.1-8745_1-8742delinsCTTT NP_002032.2:n.1-8745_1-8742delinsCTTT
NM_016655.5:c.1-8745_1-8742delinsCTTT NP_057739.1:n.1-8745_1-8742delinsCTTT
NM_181427.4:c.1-8745_1-8742delinsCTTT NP_852092.1:n.1-8745_1-8742delinsCTTT