Canonical Allele Identifier: CA1479860445
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126677_99126683delinsTTTCTTA , CM000666.2:g.99126677_99126683delinsTTTCTTA GRCh38
NC_000004.11:g.100047828_100047834delinsTTTCTTA , CM000666.1:g.100047828_100047834delinsTTTCTTA GRCh37
NC_000004.10:g.100266851_100266857delinsTTTCTTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.1029_1035delinsTAAGAAA MANE Select ENSP00000265512.7:p.Asn343=
ENST00000265512.11:c.1029_1035delinsTAAGAAA ENSP00000265512.7:p.Asn343=
ENST00000505590.5:c.1086_1092delinsTAAGAAA ENSP00000425416.1:p.Asn362=
ENST00000506705.5:c.*1003_*1009delinsTAAGAAA ENSP00000426667.1:n.*1003_*1009delinsTAAGAAA
ENST00000508393.5:c.1086_1092delinsTAAGAAA ENSP00000424630.1:p.Asn362=
ENST00000509471.5:c.383_389delinsTAAGAAA ENSP00000424583.1:n.383_389delinsTAAGAAA
ENST00000629236.2:c.1029_1035delinsTAAGAAA ENSP00000486450.1:p.Asn343=
NM_000670.3:c.1029_1035delinsTAAGAAA NP_000661.2:p.Asn343=
NM_000670.4:c.1029_1035delinsTAAGAAA NP_000661.2:p.Asn343=
NM_001306171.1:c.1086_1092delinsTAAGAAA NP_001293100.1:p.Asn362=
NM_001306172.1:c.1086_1092delinsTAAGAAA NP_001293101.1:p.Asn362=
NR_037884.1:n.429-6878_429-6872delinsTTTCTTA
XR_938685.1:n.1257_1263delinsTAAGAAA
XR_938686.1:n.1248_1254delinsTAAGAAA
XR_938687.1:n.1121_1127delinsTAAGAAA
NM_000670.5:c.1029_1035delinsTAAGAAA MANE Select NP_000661.2:p.Asn343=
NM_001306171.2:c.1086_1092delinsTAAGAAA NP_001293100.1:p.Asn362=
NM_001306172.2:c.1086_1092delinsTAAGAAA NP_001293101.1:p.Asn362=