Canonical Allele Identifier: CA357478267

Gene: ADH4

Linked Data

• dbSNP Id: rs774035712
• gnomAD v2: 4-100045575-G-T
• gnomAD v4: 4-99124424-G-T
• MyVariant Identifiers: chr4:g.100045575G>T (hg19) ; chr4:g.99124424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124424G>T , CM000666.2:g.99124424G>T	GRCh38
NC_000004.11:g.100045575G>T , CM000666.1:g.100045575G>T	GRCh37
NC_000004.10:g.100264598G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.*18C>A MANE Select	ENSP00000265512.7:n.*18C>A
ENST00000265512.11:c.*18C>A	ENSP00000265512.7:n.*18C>A
ENST00000505590.5:c.*18C>A	ENSP00000425416.1:n.*18C>A
ENST00000508393.5:c.*18C>A	ENSP00000424630.1:n.*18C>A
ENST00000509471.5:c.515C>A	ENSP00000424583.1:n.515C>A
ENST00000629236.2:c.1158C>A	ENSP00000486450.1:p.Phe386Leu
NM_000670.3:c.*18C>A	NP_000661.2:n.*18C>A
NM_000670.4:c.*18C>A	NP_000661.2:n.*18C>A
NM_001306171.1:c.*18C>A	NP_001293100.1:n.*18C>A
NM_001306172.1:c.*18C>A	NP_001293101.1:n.*18C>A
NR_037884.1:n.429-9131G>T
XR_938685.1:n.1500C>A
XR_938686.1:n.1491C>A
XR_938687.1:n.1364C>A
NM_000670.5:c.*18C>A MANE Select	NP_000661.2:n.*18C>A
NM_001306171.2:c.*18C>A	NP_001293100.1:n.*18C>A
NM_001306172.2:c.*18C>A	NP_001293101.1:n.*18C>A