Canonical Allele Identifier: CA2671525012
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420391-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420391T>C , CM000666.2:g.99420391T>C GRCh38
NC_000004.11:g.100341548T>C , CM000666.1:g.100341548T>C GRCh37
NC_000004.10:g.100560571T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.825+142A>G MANE Select ENSP00000414254.2:n.825+142A>G
ENST00000209665.8:c.861+142A>G ENSP00000209665.4:n.861+142A>G
ENST00000437033.6:c.825+142A>G ENSP00000414254.2:n.825+142A>G
ENST00000476959.5:c.885+142A>G ENSP00000420269.1:n.885+142A>G
ENST00000482593.5:c.654+142A>G ENSP00000420613.1:n.654+142A>G
NM_000673.4:c.861+142A>G NP_000664.2:n.861+142A>G
NM_001166504.1:c.885+142A>G NP_001159976.1:n.885+142A>G
NM_000673.7:c.825+142A>G MANE Select NP_000664.3:n.825+142A>G
NM_001166504.2:c.885+142A>G NP_001159976.1:n.885+142A>G
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