Canonical Allele Identifier: CA1065916063
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs1721646078

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99421022del , CM000666.2:g.99421022del GRCh38
NC_000004.11:g.100342179del , CM000666.1:g.100342179del GRCh37
NC_000004.10:g.100561202del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-225del MANE Select ENSP00000414254.2:n.565-225del
ENST00000209665.8:c.601-225del ENSP00000209665.4:n.601-225del
ENST00000437033.6:c.565-225del ENSP00000414254.2:n.565-225del
ENST00000476959.5:c.625-225del ENSP00000420269.1:n.625-225del
ENST00000482593.5:c.394-225del ENSP00000420613.1:n.394-225del
NM_000673.4:c.601-225del NP_000664.2:n.601-225del
NM_001166504.1:c.625-225del NP_001159976.1:n.625-225del
NM_000673.7:c.565-225del MANE Select NP_000664.3:n.565-225del
NM_001166504.2:c.625-225del NP_001159976.1:n.625-225del