Canonical Allele Identifier: CA2762793433
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126298_99126299insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT , CM000666.2:g.99126298_99126299insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT GRCh38
NC_000004.11:g.100047449_100047450insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT , CM000666.1:g.100047449_100047450insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT GRCh37
NC_000004.10:g.100266472_100266473insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT MANE Select ENSP00000265512.7:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGA...
ENST00000265512.11:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT ENSP00000265512.7:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGA...
ENST00000505590.5:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT ENSP00000425416.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGA...
ENST00000508393.5:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT ENSP00000424630.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGA...
ENST00000509471.5:c.472+297_472+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT ENSP00000424583.1:n.472+297_472+298insAATGTTAGATCCCTCCCTAGAAA...
ENST00000629236.2:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT ENSP00000486450.1:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGA...
NM_000670.3:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_000661.2:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGA...
NM_000670.4:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_000661.2:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGA...
NM_001306171.1:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_001293100.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAG...
NM_001306172.1:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_001293101.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAG...
NR_037884.1:n.429-7257_429-7256insTATACTACACAGAAACCTCTCTTTCTAGGGAGGGATCTAACATTAT
XR_938685.1:n.1346+297_1346+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT
XR_938686.1:n.1337+297_1337+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT
XR_938687.1:n.1210+297_1210+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT
NM_000670.5:c.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT MANE Select NP_000661.2:n.1118+297_1118+298insAATGTTAGATCCCTCCCTAGAAAGAGA...
NM_001306171.2:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_001293100.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAG...
NM_001306172.2:c.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAGAGAGGTTTCTGTGTAGTATAAT NP_001293101.1:n.1175+297_1175+298insAATGTTAGATCCCTCCCTAGAAAG...