Canonical Allele Identifier: CA1479860511
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126828T= , CM000666.2:g.99126828T= GRCh38
NC_000004.11:g.100047979T= , CM000666.1:g.100047979T= GRCh37
NC_000004.10:g.100267002T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.980-96A= MANE Select ENSP00000265512.7:n.980-96A=
ENST00000265512.11:c.980-96A= ENSP00000265512.7:n.980-96A=
ENST00000505590.5:c.1037-96A= ENSP00000425416.1:n.1037-96A=
ENST00000506705.5:c.*954-96A= ENSP00000426667.1:n.*954-96A=
ENST00000508393.5:c.1037-96A= ENSP00000424630.1:n.1037-96A=
ENST00000509471.5:c.334-96A= ENSP00000424583.1:n.334-96A=
ENST00000629236.2:c.980-96A= ENSP00000486450.1:n.980-96A=
NM_000670.3:c.980-96A= NP_000661.2:n.980-96A=
NM_000670.4:c.980-96A= NP_000661.2:n.980-96A=
NM_001306171.1:c.1037-96A= NP_001293100.1:n.1037-96A=
NM_001306172.1:c.1037-96A= NP_001293101.1:n.1037-96A=
NR_037884.1:n.429-6727T=
XR_938685.1:n.1208-96A=
XR_938686.1:n.1199-96A=
XR_938687.1:n.1072-96A=
NM_000670.5:c.980-96A= MANE Select NP_000661.2:n.980-96A=
NM_001306171.2:c.1037-96A= NP_001293100.1:n.1037-96A=
NM_001306172.2:c.1037-96A= NP_001293101.1:n.1037-96A=