Canonical Allele Identifier: CA2671506627

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124422-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124423del , CM000666.2:g.99124423del	GRCh38
NC_000004.11:g.100045574del , CM000666.1:g.100045574del	GRCh37
NC_000004.10:g.100264597del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.*19del MANE Select	ENSP00000265512.7:n.*19del
ENST00000265512.11:c.*19del	ENSP00000265512.7:n.*19del
ENST00000505590.5:c.*19del	ENSP00000425416.1:n.*19del
ENST00000508393.5:c.*19del	ENSP00000424630.1:n.*19del
ENST00000509471.5:c.516del	ENSP00000424583.1:n.516del
ENST00000629236.2:c.1159del	ENSP00000486450.1:p.Arg387GlufsTer18
NM_000670.3:c.*19del	NP_000661.2:n.*19del
NM_000670.4:c.*19del	NP_000661.2:n.*19del
NM_001306171.1:c.*19del	NP_001293100.1:n.*19del
NM_001306172.1:c.*19del	NP_001293101.1:n.*19del
NR_037884.1:n.429-9132del
XR_938685.1:n.1501del
XR_938686.1:n.1492del
XR_938687.1:n.1365del
NM_000670.5:c.*19del MANE Select	NP_000661.2:n.*19del
NM_001306171.2:c.*19del	NP_001293100.1:n.*19del
NM_001306172.2:c.*19del	NP_001293101.1:n.*19del