Canonical Allele Identifier: CA2671525472
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99428448-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428448A>C , CM000666.2:g.99428448A>C GRCh38
NC_000004.11:g.100349605A>C , CM000666.1:g.100349605A>C GRCh37
NC_000004.10:g.100568628A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.259+44T>G MANE Select ENSP00000414254.2:n.259+44T>G
ENST00000209665.8:c.295+44T>G ENSP00000209665.4:n.295+44T>G
ENST00000437033.6:c.259+44T>G ENSP00000414254.2:n.259+44T>G
ENST00000474027.1:c.88+44T>G ENSP00000420300.1:n.88+44T>G
ENST00000476959.5:c.319+44T>G ENSP00000420269.1:n.319+44T>G
ENST00000482593.5:c.88+44T>G ENSP00000420613.1:n.88+44T>G
NM_000673.4:c.295+44T>G NP_000664.2:n.295+44T>G
NM_001166504.1:c.319+44T>G NP_001159976.1:n.319+44T>G
NM_000673.7:c.259+44T>G MANE Select NP_000664.3:n.259+44T>G
NM_001166504.2:c.319+44T>G NP_001159976.1:n.319+44T>G