Canonical Allele Identifier: CA800705899

Gene: ADH4

Linked Data

• dbSNP Id: rs1353142513
• gnomAD v3: 4-99126366-G-GT
• gnomAD v4: 4-99126366-G-GT
• MyVariant Identifiers: chr4:g.100047517_100047518insT (hg19) ; chr4:g.99126366_99126367insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126367dup , CM000666.2:g.99126367dup	GRCh38
NC_000004.11:g.100047518dup , CM000666.1:g.100047518dup	GRCh37
NC_000004.10:g.100266541dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+227dup MANE Select	ENSP00000265512.7:n.1118+227dup
ENST00000265512.11:c.1118+227dup	ENSP00000265512.7:n.1118+227dup
ENST00000505590.5:c.1175+227dup	ENSP00000425416.1:n.1175+227dup
ENST00000508393.5:c.1175+227dup	ENSP00000424630.1:n.1175+227dup
ENST00000509471.5:c.472+227dup	ENSP00000424583.1:n.472+227dup
ENST00000629236.2:c.1118+227dup	ENSP00000486450.1:n.1118+227dup
NM_000670.3:c.1118+227dup	NP_000661.2:n.1118+227dup
NM_000670.4:c.1118+227dup	NP_000661.2:n.1118+227dup
NM_001306171.1:c.1175+227dup	NP_001293100.1:n.1175+227dup
NM_001306172.1:c.1175+227dup	NP_001293101.1:n.1175+227dup
NR_037884.1:n.429-7188dup
XR_938685.1:n.1346+227dup
XR_938686.1:n.1337+227dup
XR_938687.1:n.1210+227dup
NM_000670.5:c.1118+227dup MANE Select	NP_000661.2:n.1118+227dup
NM_001306171.2:c.1175+227dup	NP_001293100.1:n.1175+227dup
NM_001306172.2:c.1175+227dup	NP_001293101.1:n.1175+227dup