Canonical Allele Identifier: CA800704725

Gene: ADH4

Linked Data

• dbSNP Id: rs1452953058
• gnomAD v3: 4-99124348-C-T
• gnomAD v4: 4-99124348-C-T
• MyVariant Identifiers: chr4:g.100045499C>T (hg19) ; chr4:g.99124348C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124348C>T , CM000666.2:g.99124348C>T	GRCh38
NC_000004.11:g.100045499C>T , CM000666.1:g.100045499C>T	GRCh37
NC_000004.10:g.100264522C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*94G>A MANE Select	ENSP00000265512.7:n.*94G>A
ENST00000265512.11:c.*94G>A	ENSP00000265512.7:n.*94G>A
ENST00000508393.5:c.*94G>A	ENSP00000424630.1:n.*94G>A
ENST00000629236.2:c.*58G>A	ENSP00000486450.1:n.*58G>A
NM_000670.3:c.*94G>A	NP_000661.2:n.*94G>A
NM_000670.4:c.*94G>A	NP_000661.2:n.*94G>A
NM_001306171.1:c.*94G>A	NP_001293100.1:n.*94G>A
NM_001306172.1:c.*94G>A	NP_001293101.1:n.*94G>A
NR_037884.1:n.429-9207C>T
XR_938685.1:n.1576G>A
XR_938686.1:n.1567G>A
XR_938687.1:n.1440G>A
NM_000670.5:c.*94G>A MANE Select	NP_000661.2:n.*94G>A
NM_001306171.2:c.*94G>A	NP_001293100.1:n.*94G>A
NM_001306172.2:c.*94G>A	NP_001293101.1:n.*94G>A