Canonical Allele Identifier: CA101602180

Gene: ADH4

Linked Data

• dbSNP Id: rs3049429
• gnomAD v2: 4-100047447-C-CATT
• gnomAD v3: 4-99126296-C-CATT
• gnomAD v4: 4-99126296-C-CATT
• MyVariant Identifiers: chr4:g.100047447_100047448insATT (hg19) ; chr4:g.99126296_99126297insATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126298_99126299insTAT , CM000666.2:g.99126298_99126299insTAT	GRCh38
NC_000004.11:g.100047449_100047450insTAT , CM000666.1:g.100047449_100047450insTAT	GRCh37
NC_000004.10:g.100266472_100266473insTAT	NCBI36

Transcript Alleles

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