Canonical Allele Identifier: CA3018630
Gene: ADH4 HGNC NCBI

Linked Data

dbSNP Id: rs10009145
gnomAD v3: 4-99126778-G-A
gnomAD v4: 4-99126778-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99126778G>A , CM000666.2:g.99126778G>A GRCh38
NC_000004.11:g.100047929G>A , CM000666.1:g.100047929G>A GRCh37
NC_000004.10:g.100266952G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.980-46C>T MANE Select ENSP00000265512.7:n.980-46C>T
ENST00000265512.11:c.980-46C>T ENSP00000265512.7:n.980-46C>T
ENST00000505590.5:c.1037-46C>T ENSP00000425416.1:n.1037-46C>T
ENST00000506705.5:c.*954-46C>T ENSP00000426667.1:n.*954-46C>T
ENST00000508393.5:c.1037-46C>T ENSP00000424630.1:n.1037-46C>T
ENST00000509471.5:c.334-46C>T ENSP00000424583.1:n.334-46C>T
ENST00000629236.2:c.980-46C>T ENSP00000486450.1:n.980-46C>T
NM_000670.3:c.980-46C>T NP_000661.2:n.980-46C>T
NM_000670.4:c.980-46C>T NP_000661.2:n.980-46C>T
NM_001306171.1:c.1037-46C>T NP_001293100.1:n.1037-46C>T
NM_001306172.1:c.1037-46C>T NP_001293101.1:n.1037-46C>T
NR_037884.1:n.429-6777G>A
XR_938685.1:n.1208-46C>T
XR_938686.1:n.1199-46C>T
XR_938687.1:n.1072-46C>T
NM_000670.5:c.980-46C>T MANE Select NP_000661.2:n.980-46C>T
NM_001306171.2:c.1037-46C>T NP_001293100.1:n.1037-46C>T
NM_001306172.2:c.1037-46C>T NP_001293101.1:n.1037-46C>T