Canonical Allele Identifier: CA2706760334

Gene: ADH4

Linked Data

• dbSNP Id: rs2110490736

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127345_99127346insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA , CM000666.2:g.99127345_99127346insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA	GRCh38
NC_000004.11:g.100048496_100048497insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA , CM000666.1:g.100048496_100048497insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA	GRCh37
NC_000004.10:g.100267519_100267520insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT MANE Select	ENSP00000265512.7:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATC...
ENST00000265512.11:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000265512.7:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATC...
ENST00000505590.5:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000425416.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATC...
ENST00000506705.5:c.*818-2_*818-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000426667.1:n.*818-2_*818-1insTTTTGCCCTTGACTGTGCAGGTGGA...
ENST00000508393.5:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000424630.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATC...
ENST00000509471.5:c.334-614_334-613insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000424583.1:n.334-614_334-613insTTTTGCCCTTGACTGTGCAGGTG...
ENST00000629236.2:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	ENSP00000486450.1:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATC...
NM_000670.3:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_000661.2:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAAC...
NM_000670.4:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_000661.2:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAAC...
NM_001306171.1:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_001293100.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGA...
NM_001306172.1:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_001293101.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGA...
NR_037884.1:n.429-6210_429-6209insATGGTTTCAGATCCACCTGCACAGTCAAGGGCAAAA
XR_938685.1:n.1072-2_1072-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT
XR_938686.1:n.1063-2_1063-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT
XR_938687.1:n.936-2_936-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT
NM_000670.5:c.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT MANE Select	NP_000661.2:n.844-2_844-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAAC...
NM_001306171.2:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_001293100.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGA...
NM_001306172.2:c.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGAAACCAT	NP_001293101.1:n.901-2_901-1insTTTTGCCCTTGACTGTGCAGGTGGATCTGA...