Canonical Allele Identifier: CA2671506519
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124331-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124331G>T , CM000666.2:g.99124331G>T GRCh38
NC_000004.11:g.100045482G>T , CM000666.1:g.100045482G>T GRCh37
NC_000004.10:g.100264505G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*111C>A MANE Select ENSP00000265512.7:n.*111C>A
ENST00000265512.11:c.*111C>A ENSP00000265512.7:n.*111C>A
ENST00000508393.5:c.*111C>A ENSP00000424630.1:n.*111C>A
ENST00000629236.2:c.*75C>A ENSP00000486450.1:n.*75C>A
NM_000670.3:c.*111C>A NP_000661.2:n.*111C>A
NM_000670.4:c.*111C>A NP_000661.2:n.*111C>A
NM_001306171.1:c.*111C>A NP_001293100.1:n.*111C>A
NM_001306172.1:c.*111C>A NP_001293101.1:n.*111C>A
NR_037884.1:n.429-9224G>T
XR_938685.1:n.1593C>A
XR_938686.1:n.1584C>A
XR_938687.1:n.1457C>A
NM_000670.5:c.*111C>A MANE Select NP_000661.2:n.*111C>A
NM_001306171.2:c.*111C>A NP_001293100.1:n.*111C>A
NM_001306172.2:c.*111C>A NP_001293101.1:n.*111C>A
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