Canonical Allele Identifier: CA1930505032
Gene: HOGA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97598979T= , CM000672.2:g.97598979T= GRCh38
NC_000010.10:g.99358736T= , CM000672.1:g.99358736T= GRCh37
NC_000010.9:g.99348726T= NCBI36
NG_027922.1:g.19635T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.340+76T= MANE Select ENSP00000359680.4:n.340+76T=
ENST00000370646.8:c.340+76T= ENSP00000359680.4:n.340+76T=
ENST00000370647.8:c.212-2878T= ENSP00000359681.4:n.212-2878T=
ENST00000370649.3:c.212-2878T= ENSP00000359683.3:n.212-2878T=
ENST00000465608.1:n.721+76T=
NM_001134670.1:c.212-2878T= NP_001128142.1:n.212-2878T=
NM_138413.3:c.340+76T= NP_612422.2:n.340+76T=
NM_138413.4:c.340+76T= MANE Select NP_612422.2:n.340+76T=
NM_001134670.2:c.212-2878T= NP_001128142.1:n.212-2878T=
Search 100 bp 5'
Search 100 bp 3'