Canonical Allele Identifier: CA1479860749

Gene: ADH4

Linked Data

• dbSNP Id: rs1729133416

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127365del , CM000666.2:g.99127365del	GRCh38
NC_000004.11:g.100048516del , CM000666.1:g.100048516del	GRCh37
NC_000004.10:g.100267539del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.844-20del MANE Select	ENSP00000265512.7:n.844-20del
ENST00000265512.11:c.844-20del	ENSP00000265512.7:n.844-20del
ENST00000505590.5:c.901-20del	ENSP00000425416.1:n.901-20del
ENST00000506705.5:c.*818-20del	ENSP00000426667.1:n.*818-20del
ENST00000508393.5:c.901-20del	ENSP00000424630.1:n.901-20del
ENST00000509471.5:c.334-632del	ENSP00000424583.1:n.334-632del
ENST00000629236.2:c.844-20del	ENSP00000486450.1:n.844-20del
NM_000670.3:c.844-20del	NP_000661.2:n.844-20del
NM_000670.4:c.844-20del	NP_000661.2:n.844-20del
NM_001306171.1:c.901-20del	NP_001293100.1:n.901-20del
NM_001306172.1:c.901-20del	NP_001293101.1:n.901-20del
NR_037884.1:n.429-6190del
XR_938685.1:n.1072-20del
XR_938686.1:n.1063-20del
XR_938687.1:n.936-20del
NM_000670.5:c.844-20del MANE Select	NP_000661.2:n.844-20del
NM_001306171.2:c.901-20del	NP_001293100.1:n.901-20del
NM_001306172.2:c.901-20del	NP_001293101.1:n.901-20del