Canonical Allele Identifier: CA1555781460
Gene: HEXB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74718747_74718750delinsTCTA , CM000667.2:g.74718747_74718750delinsTCTA GRCh38
NC_000005.9:g.74014572_74014575delinsTCTA , CM000667.1:g.74014572_74014575delinsTCTA GRCh37
NC_000005.8:g.74050328_74050331delinsTCTA NCBI36
NG_009770.1:g.38604_38607delinsTCTA
NG_009770.2:g.83725_83728delinsTCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000261416.12:c.1243-50_1243-47delinsTCTA MANE Select ENSP00000261416.7:n.1243-50_1243-47delins...
ENST00000261416.11:c.1243-50_1243-47delinsTCTA ENSP00000261416.7:n.1243-50_1243-47delins...
ENST00000503312.5:c.119-50_119-47delinsTCTA
ENST00000504459.5:n.440-50_440-47delinsTCTA
ENST00000511181.5:c.568-50_568-47delinsTCTA ENSP00000426285.1:n.568-50_568-47delinsTC...
ENST00000513336.5:c.179-50_179-47delinsTCTA
ENST00000513539.1:n.74-162_74-159delinsTCTA
NM_000521.3:c.1243-50_1243-47delinsTCTA NP_000512.1:n.1243-50_1243-47delinsTCTA
NM_001292004.1:c.568-50_568-47delinsTCTA NP_001278933.1:n.568-50_568-47delinsTCTA
NM_000521.4:c.1243-50_1243-47delinsTCTA MANE Select NP_000512.2:n.1243-50_1243-47delinsTCTA
NM_001292004.2:c.568-50_568-47delinsTCTA NP_001278933.1:n.568-50_568-47delinsTCTA