Canonical Allele Identifier: CA800704718

Gene: ADH4

Linked Data

• dbSNP Id: rs1173614882
• gnomAD v4: 4-99124341-G-C
• MyVariant Identifiers: chr4:g.100045492G>C (hg19) ; chr4:g.99124341G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124341G>C , CM000666.2:g.99124341G>C	GRCh38
NC_000004.11:g.100045492G>C , CM000666.1:g.100045492G>C	GRCh37
NC_000004.10:g.100264515G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*101C>G MANE Select	ENSP00000265512.7:n.*101C>G
ENST00000265512.11:c.*101C>G	ENSP00000265512.7:n.*101C>G
ENST00000508393.5:c.*101C>G	ENSP00000424630.1:n.*101C>G
ENST00000629236.2:c.*65C>G	ENSP00000486450.1:n.*65C>G
NM_000670.3:c.*101C>G	NP_000661.2:n.*101C>G
NM_000670.4:c.*101C>G	NP_000661.2:n.*101C>G
NM_001306171.1:c.*101C>G	NP_001293100.1:n.*101C>G
NM_001306172.1:c.*101C>G	NP_001293101.1:n.*101C>G
NR_037884.1:n.429-9214G>C
XR_938685.1:n.1583C>G
XR_938686.1:n.1574C>G
XR_938687.1:n.1447C>G
NM_000670.5:c.*101C>G MANE Select	NP_000661.2:n.*101C>G
NM_001306171.2:c.*101C>G	NP_001293100.1:n.*101C>G
NM_001306172.2:c.*101C>G	NP_001293101.1:n.*101C>G