Canonical Allele Identifier: CA553095876

Gene: ADH4

Linked Data

• gnomAD v2: 4-100048344-G-GAAA
• gnomAD v4: 4-99127193-G-GAAA
• MyVariant Identifiers: chr4:g.100048345_100048346insAAA (hg19) ; chr4:g.99127194_99127195insAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127201_99127203dup , CM000666.2:g.99127201_99127203dup	GRCh38
NC_000004.11:g.100048352_100048354dup , CM000666.1:g.100048352_100048354dup	GRCh37
NC_000004.10:g.100267375_100267377dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+13_979+15dup MANE Select	ENSP00000265512.7:n.979+13_979+15dup
ENST00000265512.11:c.979+13_979+15dup	ENSP00000265512.7:n.979+13_979+15dup
ENST00000505590.5:c.1036+13_1036+15dup	ENSP00000425416.1:n.1036+13_1036+15dup
ENST00000506705.5:c.*953+13_*953+15dup	ENSP00000426667.1:n.*953+13_*953+15dup
ENST00000508393.5:c.1036+13_1036+15dup	ENSP00000424630.1:n.1036+13_1036+15dup
ENST00000509471.5:c.334-464_334-462dup	ENSP00000424583.1:n.334-464_334-462dup
ENST00000629236.2:c.979+13_979+15dup	ENSP00000486450.1:n.979+13_979+15dup
NM_000670.3:c.979+13_979+15dup	NP_000661.2:n.979+13_979+15dup
NM_000670.4:c.979+13_979+15dup	NP_000661.2:n.979+13_979+15dup
NM_001306171.1:c.1036+13_1036+15dup	NP_001293100.1:n.1036+13_1036+15dup
NM_001306172.1:c.1036+13_1036+15dup	NP_001293101.1:n.1036+13_1036+15dup
NR_037884.1:n.429-6354_429-6352dup
XR_938685.1:n.1207+13_1207+15dup
XR_938686.1:n.1198+13_1198+15dup
XR_938687.1:n.1071+13_1071+15dup
NM_000670.5:c.979+13_979+15dup MANE Select	NP_000661.2:n.979+13_979+15dup
NM_001306171.2:c.1036+13_1036+15dup	NP_001293100.1:n.1036+13_1036+15dup
NM_001306172.2:c.1036+13_1036+15dup	NP_001293101.1:n.1036+13_1036+15dup