Canonical Allele Identifier: CA357480231
Gene: ADH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99127342T>A , CM000666.2:g.99127342T>A GRCh38
NC_000004.11:g.100048493T>A , CM000666.1:g.100048493T>A GRCh37
NC_000004.10:g.100267516T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.846A>T MANE Select ENSP00000265512.7:p.Lys282Asn
ENST00000265512.11:c.846A>T ENSP00000265512.7:p.Lys282Asn
ENST00000505590.5:c.903A>T ENSP00000425416.1:p.Lys301Asn
ENST00000506705.5:c.*820A>T ENSP00000426667.1:n.*820A>T
ENST00000508393.5:c.903A>T ENSP00000424630.1:p.Lys301Asn
ENST00000509471.5:c.334-610A>T ENSP00000424583.1:n.334-610A>T
ENST00000629236.2:c.846A>T ENSP00000486450.1:p.Lys282Asn
NM_000670.3:c.846A>T NP_000661.2:p.Lys282Asn
NM_000670.4:c.846A>T NP_000661.2:p.Lys282Asn
NM_001306171.1:c.903A>T NP_001293100.1:p.Lys301Asn
NM_001306172.1:c.903A>T NP_001293101.1:p.Lys301Asn
NR_037884.1:n.429-6213T>A
XR_938685.1:n.1074A>T
XR_938686.1:n.1065A>T
XR_938687.1:n.938A>T
NM_000670.5:c.846A>T MANE Select NP_000661.2:p.Lys282Asn
NM_001306171.2:c.903A>T NP_001293100.1:p.Lys301Asn
NM_001306172.2:c.903A>T NP_001293101.1:p.Lys301Asn