Canonical Allele Identifier: CA1479860658

Gene: ADH4

Linked Data

• dbSNP Id: rs1729123802
• gnomAD v4: 4-99127192-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127193del , CM000666.2:g.99127193del	GRCh38
NC_000004.11:g.100048344del , CM000666.1:g.100048344del	GRCh37
NC_000004.10:g.100267367del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+16del MANE Select	ENSP00000265512.7:n.979+16del
ENST00000265512.11:c.979+16del	ENSP00000265512.7:n.979+16del
ENST00000505590.5:c.1036+16del	ENSP00000425416.1:n.1036+16del
ENST00000506705.5:c.*953+16del	ENSP00000426667.1:n.*953+16del
ENST00000508393.5:c.1036+16del	ENSP00000424630.1:n.1036+16del
ENST00000509471.5:c.334-461del	ENSP00000424583.1:n.334-461del
ENST00000629236.2:c.979+16del	ENSP00000486450.1:n.979+16del
NM_000670.3:c.979+16del	NP_000661.2:n.979+16del
NM_000670.4:c.979+16del	NP_000661.2:n.979+16del
NM_001306171.1:c.1036+16del	NP_001293100.1:n.1036+16del
NM_001306172.1:c.1036+16del	NP_001293101.1:n.1036+16del
NR_037884.1:n.429-6362del
XR_938685.1:n.1207+16del
XR_938686.1:n.1198+16del
XR_938687.1:n.1071+16del
NM_000670.5:c.979+16del MANE Select	NP_000661.2:n.979+16del
NM_001306171.2:c.1036+16del	NP_001293100.1:n.1036+16del
NM_001306172.2:c.1036+16del	NP_001293101.1:n.1036+16del