Canonical Allele Identifier: CA2671506630

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124434-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124436del , CM000666.2:g.99124436del	GRCh38
NC_000004.11:g.100045587del , CM000666.1:g.100045587del	GRCh37
NC_000004.10:g.100264610del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.*7del MANE Select	ENSP00000265512.7:n.*7del
ENST00000265512.11:c.*7del	ENSP00000265512.7:n.*7del
ENST00000505590.5:c.*7del	ENSP00000425416.1:n.*7del
ENST00000508393.5:c.*7del	ENSP00000424630.1:n.*7del
ENST00000509471.5:c.504del	ENSP00000424583.1:n.504del
ENST00000629236.2:c.1147del	ENSP00000486450.1:p.Gln383ArgfsTer22
NM_000670.3:c.*7del	NP_000661.2:n.*7del
NM_000670.4:c.*7del	NP_000661.2:n.*7del
NM_001306171.1:c.*7del	NP_001293100.1:n.*7del
NM_001306172.1:c.*7del	NP_001293101.1:n.*7del
NR_037884.1:n.429-9119del
XR_938685.1:n.1489del
XR_938686.1:n.1480del
XR_938687.1:n.1353del
NM_000670.5:c.*7del MANE Select	NP_000661.2:n.*7del
NM_001306171.2:c.*7del	NP_001293100.1:n.*7del
NM_001306172.2:c.*7del	NP_001293101.1:n.*7del