Canonical Allele Identifier: CA800704944

Gene: ADH4

Linked Data

• dbSNP Id: rs1199056048
• MyVariant Identifiers: chr4:g.100045789del (hg19) ; chr4:g.99124638del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124639del , CM000666.2:g.99124639del	GRCh38
NC_000004.11:g.100045790del , CM000666.1:g.100045790del	GRCh37
NC_000004.10:g.100264813del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1119-172del MANE Select	ENSP00000265512.7:n.1119-172del
ENST00000265512.11:c.1119-172del	ENSP00000265512.7:n.1119-172del
ENST00000505590.5:c.1176-172del	ENSP00000425416.1:n.1176-172del
ENST00000508393.5:c.1176-172del	ENSP00000424630.1:n.1176-172del
ENST00000509471.5:c.473-172del	ENSP00000424583.1:n.473-172del
ENST00000629236.2:c.1119-172del	ENSP00000486450.1:n.1119-172del
NM_000670.3:c.1119-172del	NP_000661.2:n.1119-172del
NM_000670.4:c.1119-172del	NP_000661.2:n.1119-172del
NM_001306171.1:c.1176-172del	NP_001293100.1:n.1176-172del
NM_001306172.1:c.1176-172del	NP_001293101.1:n.1176-172del
NR_037884.1:n.429-8916del
XR_938685.1:n.1457+54del
XR_938686.1:n.1448+54del
XR_938687.1:n.1321+54del
NM_000670.5:c.1119-172del MANE Select	NP_000661.2:n.1119-172del
NM_001306171.2:c.1176-172del	NP_001293100.1:n.1176-172del
NM_001306172.2:c.1176-172del	NP_001293101.1:n.1176-172del