Canonical Allele Identifier: CA1065906968
Gene: ADH4 HGNC NCBI

Linked Data

dbSNP Id: rs1729024450

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124639_99124641del , CM000666.2:g.99124639_99124641del GRCh38
NC_000004.11:g.100045790_100045792del , CM000666.1:g.100045790_100045792del GRCh37
NC_000004.10:g.100264813_100264815del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.1119-170_1119-168del MANE Select ENSP00000265512.7:n.1119-170_1119-168del
ENST00000265512.11:c.1119-170_1119-168del ENSP00000265512.7:n.1119-170_1119-168del
ENST00000505590.5:c.1176-170_1176-168del ENSP00000425416.1:n.1176-170_1176-168del
ENST00000508393.5:c.1176-170_1176-168del ENSP00000424630.1:n.1176-170_1176-168del
ENST00000509471.5:c.473-170_473-168del ENSP00000424583.1:n.473-170_473-168del
ENST00000629236.2:c.1119-170_1119-168del ENSP00000486450.1:n.1119-170_1119-168del
NM_000670.3:c.1119-170_1119-168del NP_000661.2:n.1119-170_1119-168del
NM_000670.4:c.1119-170_1119-168del NP_000661.2:n.1119-170_1119-168del
NM_001306171.1:c.1176-170_1176-168del NP_001293100.1:n.1176-170_1176-168del
NM_001306172.1:c.1176-170_1176-168del NP_001293101.1:n.1176-170_1176-168del
NR_037884.1:n.429-8916_429-8914del
XR_938685.1:n.1457+56_1457+58del
XR_938686.1:n.1448+56_1448+58del
XR_938687.1:n.1321+56_1321+58del
NM_000670.5:c.1119-170_1119-168del MANE Select NP_000661.2:n.1119-170_1119-168del
NM_001306171.2:c.1176-170_1176-168del NP_001293100.1:n.1176-170_1176-168del
NM_001306172.2:c.1176-170_1176-168del NP_001293101.1:n.1176-170_1176-168del