Canonical Allele Identifier: CA1480005170
Gene: ADH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428415C= , CM000666.2:g.99428415C= GRCh38
NC_000004.11:g.100349572C= , CM000666.1:g.100349572C= GRCh37
NC_000004.10:g.100568595C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.259+77G= MANE Select ENSP00000414254.2:n.259+77G=
ENST00000209665.8:c.295+77G= ENSP00000209665.4:n.295+77G=
ENST00000437033.6:c.259+77G= ENSP00000414254.2:n.259+77G=
ENST00000474027.1:c.88+77G= ENSP00000420300.1:n.88+77G=
ENST00000476959.5:c.319+77G= ENSP00000420269.1:n.319+77G=
ENST00000482593.5:c.88+77G= ENSP00000420613.1:n.88+77G=
NM_000673.4:c.295+77G= NP_000664.2:n.295+77G=
NM_001166504.1:c.319+77G= NP_001159976.1:n.319+77G=
NM_000673.7:c.259+77G= MANE Select NP_000664.3:n.259+77G=
NM_001166504.2:c.319+77G= NP_001159976.1:n.319+77G=
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