Canonical Allele Identifier: CA1065907568
Gene: ADH4 HGNC NCBI

Linked Data

dbSNP Id: rs1729086221

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126295_99126296insTAT , CM000666.2:g.99126295_99126296insTAT GRCh38
NC_000004.11:g.100047446_100047447insTAT , CM000666.1:g.100047446_100047447insTAT GRCh37
NC_000004.10:g.100266469_100266470insTAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.1118+298_1118+299insATA MANE Select ENSP00000265512.7:n.1118+298_1118+299insATA
ENST00000265512.11:c.1118+298_1118+299insATA ENSP00000265512.7:n.1118+298_1118+299insATA
ENST00000505590.5:c.1175+298_1175+299insATA ENSP00000425416.1:n.1175+298_1175+299insATA
ENST00000508393.5:c.1175+298_1175+299insATA ENSP00000424630.1:n.1175+298_1175+299insATA
ENST00000509471.5:c.472+298_472+299insATA ENSP00000424583.1:n.472+298_472+299insATA
ENST00000629236.2:c.1118+298_1118+299insATA ENSP00000486450.1:n.1118+298_1118+299insATA
NM_000670.3:c.1118+298_1118+299insATA NP_000661.2:n.1118+298_1118+299insATA
NM_000670.4:c.1118+298_1118+299insATA NP_000661.2:n.1118+298_1118+299insATA
NM_001306171.1:c.1175+298_1175+299insATA NP_001293100.1:n.1175+298_1175+299insATA
NM_001306172.1:c.1175+298_1175+299insATA NP_001293101.1:n.1175+298_1175+299insATA
NR_037884.1:n.429-7260_429-7259insTAT
XR_938685.1:n.1346+298_1346+299insATA
XR_938686.1:n.1337+298_1337+299insATA
XR_938687.1:n.1210+298_1210+299insATA
NM_000670.5:c.1118+298_1118+299insATA MANE Select NP_000661.2:n.1118+298_1118+299insATA
NM_001306171.2:c.1175+298_1175+299insATA NP_001293100.1:n.1175+298_1175+299insATA
NM_001306172.2:c.1175+298_1175+299insATA NP_001293101.1:n.1175+298_1175+299insATA