Canonical Allele Identifier: CA2671507105

Gene: ADH4

Linked Data

• gnomAD v4: 4-99127331-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127333del , CM000666.2:g.99127333del	GRCh38
NC_000004.11:g.100048484del , CM000666.1:g.100048484del	GRCh37
NC_000004.10:g.100267507del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.856del MANE Select	ENSP00000265512.7:p.Asp286ThrfsTer15
ENST00000265512.11:c.856del	ENSP00000265512.7:p.Asp286ThrfsTer15
ENST00000505590.5:c.913del	ENSP00000425416.1:p.Asp305ThrfsTer15
ENST00000506705.5:c.*830del	ENSP00000426667.1:n.*830del
ENST00000508393.5:c.913del	ENSP00000424630.1:p.Asp305ThrfsTer15
ENST00000509471.5:c.334-600del	ENSP00000424583.1:n.334-600del
ENST00000629236.2:c.856del	ENSP00000486450.1:p.Asp286ThrfsTer15
NM_000670.3:c.856del	NP_000661.2:p.Asp286ThrfsTer15
NM_000670.4:c.856del	NP_000661.2:p.Asp286ThrfsTer15
NM_001306171.1:c.913del	NP_001293100.1:p.Asp305ThrfsTer15
NM_001306172.1:c.913del	NP_001293101.1:p.Asp305ThrfsTer15
NR_037884.1:n.429-6222del
XR_938685.1:n.1084del
XR_938686.1:n.1075del
XR_938687.1:n.948del
NM_000670.5:c.856del MANE Select	NP_000661.2:p.Asp286ThrfsTer15
NM_001306171.2:c.913del	NP_001293100.1:p.Asp305ThrfsTer15
NM_001306172.2:c.913del	NP_001293101.1:p.Asp305ThrfsTer15