Canonical Allele Identifier: CA1479860730

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127336_99127339delinsGGCT , CM000666.2:g.99127336_99127339delinsGGCT	GRCh38
NC_000004.11:g.100048487_100048490delinsGGCT , CM000666.1:g.100048487_100048490delinsGGCT	GRCh37
NC_000004.10:g.100267510_100267513delinsGGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.849_852delinsAGCC MANE Select	ENSP00000265512.7:p.Ala283=
ENST00000265512.11:c.849_852delinsAGCC	ENSP00000265512.7:p.Ala283=
ENST00000505590.5:c.906_909delinsAGCC	ENSP00000425416.1:p.Ala302=
ENST00000506705.5:c.*823_*826delinsAGCC	ENSP00000426667.1:n.*823_*826delinsAGCC
ENST00000508393.5:c.906_909delinsAGCC	ENSP00000424630.1:p.Ala302=
ENST00000509471.5:c.334-607_334-604delinsAGCC	ENSP00000424583.1:n.334-607_334-604delinsAGCC
ENST00000629236.2:c.849_852delinsAGCC	ENSP00000486450.1:p.Ala283=
NM_000670.3:c.849_852delinsAGCC	NP_000661.2:p.Ala283=
NM_000670.4:c.849_852delinsAGCC	NP_000661.2:p.Ala283=
NM_001306171.1:c.906_909delinsAGCC	NP_001293100.1:p.Ala302=
NM_001306172.1:c.906_909delinsAGCC	NP_001293101.1:p.Ala302=
NR_037884.1:n.429-6219_429-6216delinsGGCT
XR_938685.1:n.1077_1080delinsAGCC
XR_938686.1:n.1068_1071delinsAGCC
XR_938687.1:n.941_944delinsAGCC
NM_000670.5:c.849_852delinsAGCC MANE Select	NP_000661.2:p.Ala283=
NM_001306171.2:c.906_909delinsAGCC	NP_001293100.1:p.Ala302=
NM_001306172.2:c.906_909delinsAGCC	NP_001293101.1:p.Ala302=