Canonical Allele Identifier: CA553095880

Gene: ADH4

Linked Data

• dbSNP Id: rs1366568899
• gnomAD v2: 4-100048537-T-C
• gnomAD v4: 4-99127386-T-C
• MyVariant Identifiers: chr4:g.100048537T>C (hg19) ; chr4:g.99127386T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127386T>C , CM000666.2:g.99127386T>C	GRCh38
NC_000004.11:g.100048537T>C , CM000666.1:g.100048537T>C	GRCh37
NC_000004.10:g.100267560T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.844-42A>G MANE Select	ENSP00000265512.7:n.844-42A>G
ENST00000265512.11:c.844-42A>G	ENSP00000265512.7:n.844-42A>G
ENST00000505590.5:c.901-42A>G	ENSP00000425416.1:n.901-42A>G
ENST00000506705.5:c.*818-42A>G	ENSP00000426667.1:n.*818-42A>G
ENST00000508393.5:c.901-42A>G	ENSP00000424630.1:n.901-42A>G
ENST00000509471.5:c.334-654A>G	ENSP00000424583.1:n.334-654A>G
ENST00000629236.2:c.844-42A>G	ENSP00000486450.1:n.844-42A>G
NM_000670.3:c.844-42A>G	NP_000661.2:n.844-42A>G
NM_000670.4:c.844-42A>G	NP_000661.2:n.844-42A>G
NM_001306171.1:c.901-42A>G	NP_001293100.1:n.901-42A>G
NM_001306172.1:c.901-42A>G	NP_001293101.1:n.901-42A>G
NR_037884.1:n.429-6169T>C
XR_938685.1:n.1072-42A>G
XR_938686.1:n.1063-42A>G
XR_938687.1:n.936-42A>G
NM_000670.5:c.844-42A>G MANE Select	NP_000661.2:n.844-42A>G
NM_001306171.2:c.901-42A>G	NP_001293100.1:n.901-42A>G
NM_001306172.2:c.901-42A>G	NP_001293101.1:n.901-42A>G