Canonical Allele Identifier: CA1930506472
Gene: HOGA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97599823C= , CM000672.2:g.97599823C= GRCh38
NC_000010.10:g.99359580C= , CM000672.1:g.99359580C= GRCh37
NC_000010.9:g.99349570C= NCBI36
NG_027922.1:g.20479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370646.9:c.603+9C= MANE Select ENSP00000359680.4:n.603+9C=
ENST00000370642.4:c.13+9C=
ENST00000370646.8:c.603+9C= ENSP00000359680.4:n.603+9C=
ENST00000370647.8:c.212-2034C= ENSP00000359681.4:n.212-2034C=
ENST00000370649.3:c.212-2034C= ENSP00000359683.3:n.212-2034C=
ENST00000465608.1:n.1456C=
NM_001134670.1:c.212-2034C= NP_001128142.1:n.212-2034C=
NM_138413.3:c.603+9C= NP_612422.2:n.603+9C=
NM_138413.4:c.603+9C= MANE Select NP_612422.2:n.603+9C=
NM_001134670.2:c.212-2034C= NP_001128142.1:n.212-2034C=
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