Canonical Allele Identifier: CA2671506540
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124339-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124339T>G , CM000666.2:g.99124339T>G GRCh38
NC_000004.11:g.100045490T>G , CM000666.1:g.100045490T>G GRCh37
NC_000004.10:g.100264513T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.*103A>C MANE Select ENSP00000265512.7:n.*103A>C
ENST00000265512.11:c.*103A>C ENSP00000265512.7:n.*103A>C
ENST00000508393.5:c.*103A>C ENSP00000424630.1:n.*103A>C
ENST00000629236.2:c.*67A>C ENSP00000486450.1:n.*67A>C
NM_000670.3:c.*103A>C NP_000661.2:n.*103A>C
NM_000670.4:c.*103A>C NP_000661.2:n.*103A>C
NM_001306171.1:c.*103A>C NP_001293100.1:n.*103A>C
NM_001306172.1:c.*103A>C NP_001293101.1:n.*103A>C
NR_037884.1:n.429-9216T>G
XR_938685.1:n.1585A>C
XR_938686.1:n.1576A>C
XR_938687.1:n.1449A>C
NM_000670.5:c.*103A>C MANE Select NP_000661.2:n.*103A>C
NM_001306171.2:c.*103A>C NP_001293100.1:n.*103A>C
NM_001306172.2:c.*103A>C NP_001293101.1:n.*103A>C