Canonical Allele Identifier: CA357479955

Gene: ADH4

Linked Data

• gnomAD v4: 4-99127310-C-T
• MyVariant Identifiers: chr4:g.100048461C>T (hg19) ; chr4:g.99127310C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127310C>T , CM000666.2:g.99127310C>T	GRCh38
NC_000004.11:g.100048461C>T , CM000666.1:g.100048461C>T	GRCh37
NC_000004.10:g.100267484C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.878G>A MANE Select	ENSP00000265512.7:p.Gly293Glu
ENST00000265512.11:c.878G>A	ENSP00000265512.7:p.Gly293Glu
ENST00000505590.5:c.935G>A	ENSP00000425416.1:p.Gly312Glu
ENST00000506705.5:c.*852G>A	ENSP00000426667.1:n.*852G>A
ENST00000508393.5:c.935G>A	ENSP00000424630.1:p.Gly312Glu
ENST00000509471.5:c.334-578G>A	ENSP00000424583.1:n.334-578G>A
ENST00000629236.2:c.878G>A	ENSP00000486450.1:p.Gly293Glu
NM_000670.3:c.878G>A	NP_000661.2:p.Gly293Glu
NM_000670.4:c.878G>A	NP_000661.2:p.Gly293Glu
NM_001306171.1:c.935G>A	NP_001293100.1:p.Gly312Glu
NM_001306172.1:c.935G>A	NP_001293101.1:p.Gly312Glu
NR_037884.1:n.429-6245C>T
XR_938685.1:n.1106G>A
XR_938686.1:n.1097G>A
XR_938687.1:n.970G>A
NM_000670.5:c.878G>A MANE Select	NP_000661.2:p.Gly293Glu
NM_001306171.2:c.935G>A	NP_001293100.1:p.Gly312Glu
NM_001306172.2:c.935G>A	NP_001293101.1:p.Gly312Glu