Canonical Allele Identifier: CA1861285895
Gene: GOLM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.86078591_86078595delinsTGAGA , CM000671.2:g.86078591_86078595delinsTGAGA GRCh38
NC_000009.11:g.88693506_88693510delinsTGAGA , CM000671.1:g.88693506_88693510delinsTGAGA GRCh37
NC_000009.10:g.87883326_87883330delinsTGAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000388711.7:c.129+597_129+601delinsTCTCA ENSP00000373363.3:n.129+597_129+601delinsTCTCA
ENST00000388712.7:c.129+597_129+601delinsTCTCA MANE Select ENSP00000373364.3:n.129+597_129+601delinsTCTCA
ENST00000466178.1:c.129+597_129+601delinsTCTCA ENSP00000418155.1:n.129+597_129+601delinsTCTCA
ENST00000470762.6:c.129+597_129+601delinsTCTCA ENSP00000417504.2:n.129+597_129+601delinsTCTCA
ENST00000472919.1:n.190+706_190+710delinsTCTCA
ENST00000486130.5:c.129+597_129+601delinsTCTCA ENSP00000419076.1:n.129+597_129+601delinsTCTCA
NM_016548.3:c.129+597_129+601delinsTCTCA NP_057632.2:n.129+597_129+601delinsTCTCA
NM_177937.2:c.129+597_129+601delinsTCTCA NP_808800.1:n.129+597_129+601delinsTCTCA
NM_016548.4:c.129+597_129+601delinsTCTCA MANE Select NP_057632.2:n.129+597_129+601delinsTCTCA
NM_177937.3:c.129+597_129+601delinsTCTCA NP_808800.1:n.129+597_129+601delinsTCTCA