Canonical Allele Identifier: CA1479860530
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126886_99126888delinsATT , CM000666.2:g.99126886_99126888delinsATT GRCh38
NC_000004.11:g.100048037_100048039delinsATT , CM000666.1:g.100048037_100048039delinsATT GRCh37
NC_000004.10:g.100267060_100267062delinsATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.980-156_980-154delinsAAT MANE Select ENSP00000265512.7:n.980-156_980-154delinsAAT
ENST00000265512.11:c.980-156_980-154delinsAAT ENSP00000265512.7:n.980-156_980-154delinsAAT
ENST00000505590.5:c.1037-156_1037-154delinsAAT ENSP00000425416.1:n.1037-156_1037-154delinsAAT
ENST00000506705.5:c.*954-156_*954-154delinsAAT ENSP00000426667.1:n.*954-156_*954-154delinsAAT
ENST00000508393.5:c.1037-156_1037-154delinsAAT ENSP00000424630.1:n.1037-156_1037-154delinsAAT
ENST00000509471.5:c.334-156_334-154delinsAAT ENSP00000424583.1:n.334-156_334-154delinsAAT
ENST00000629236.2:c.980-156_980-154delinsAAT ENSP00000486450.1:n.980-156_980-154delinsAAT
NM_000670.3:c.980-156_980-154delinsAAT NP_000661.2:n.980-156_980-154delinsAAT
NM_000670.4:c.980-156_980-154delinsAAT NP_000661.2:n.980-156_980-154delinsAAT
NM_001306171.1:c.1037-156_1037-154delinsAAT NP_001293100.1:n.1037-156_1037-154delinsAAT
NM_001306172.1:c.1037-156_1037-154delinsAAT NP_001293101.1:n.1037-156_1037-154delinsAAT
NR_037884.1:n.429-6669_429-6667delinsATT
XR_938685.1:n.1208-156_1208-154delinsAAT
XR_938686.1:n.1199-156_1199-154delinsAAT
XR_938687.1:n.1072-156_1072-154delinsAAT
NM_000670.5:c.980-156_980-154delinsAAT MANE Select NP_000661.2:n.980-156_980-154delinsAAT
NM_001306171.2:c.1037-156_1037-154delinsAAT NP_001293100.1:n.1037-156_1037-154delinsAAT
NM_001306172.2:c.1037-156_1037-154delinsAAT NP_001293101.1:n.1037-156_1037-154delinsAAT