Canonical Allele Identifier: CA800706529

Gene: ADH4

Linked Data

• dbSNP Id: rs768280325
• gnomAD v3: 4-99127020-G-T
• gnomAD v4: 4-99127020-G-T
• MyVariant Identifiers: chr4:g.100048171G>T (hg19) ; chr4:g.99127020G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127020G>T , CM000666.2:g.99127020G>T	GRCh38
NC_000004.11:g.100048171G>T , CM000666.1:g.100048171G>T	GRCh37
NC_000004.10:g.100267194G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+189C>A MANE Select	ENSP00000265512.7:n.979+189C>A
ENST00000265512.11:c.979+189C>A	ENSP00000265512.7:n.979+189C>A
ENST00000505590.5:c.1036+189C>A	ENSP00000425416.1:n.1036+189C>A
ENST00000506705.5:c.*953+189C>A	ENSP00000426667.1:n.*953+189C>A
ENST00000508393.5:c.1036+189C>A	ENSP00000424630.1:n.1036+189C>A
ENST00000509471.5:c.334-288C>A	ENSP00000424583.1:n.334-288C>A
ENST00000629236.2:c.979+189C>A	ENSP00000486450.1:n.979+189C>A
NM_000670.3:c.979+189C>A	NP_000661.2:n.979+189C>A
NM_000670.4:c.979+189C>A	NP_000661.2:n.979+189C>A
NM_001306171.1:c.1036+189C>A	NP_001293100.1:n.1036+189C>A
NM_001306172.1:c.1036+189C>A	NP_001293101.1:n.1036+189C>A
NR_037884.1:n.429-6535G>T
XR_938685.1:n.1207+189C>A
XR_938686.1:n.1198+189C>A
XR_938687.1:n.1071+189C>A
NM_000670.5:c.979+189C>A MANE Select	NP_000661.2:n.979+189C>A
NM_001306171.2:c.1036+189C>A	NP_001293100.1:n.1036+189C>A
NM_001306172.2:c.1036+189C>A	NP_001293101.1:n.1036+189C>A