Canonical Allele Identifier: CA2671506542

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124340-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124340T>G , CM000666.2:g.99124340T>G	GRCh38
NC_000004.11:g.100045491T>G , CM000666.1:g.100045491T>G	GRCh37
NC_000004.10:g.100264514T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*102A>C MANE Select	ENSP00000265512.7:n.*102A>C
ENST00000265512.11:c.*102A>C	ENSP00000265512.7:n.*102A>C
ENST00000508393.5:c.*102A>C	ENSP00000424630.1:n.*102A>C
ENST00000629236.2:c.*66A>C	ENSP00000486450.1:n.*66A>C
NM_000670.3:c.*102A>C	NP_000661.2:n.*102A>C
NM_000670.4:c.*102A>C	NP_000661.2:n.*102A>C
NM_001306171.1:c.*102A>C	NP_001293100.1:n.*102A>C
NM_001306172.1:c.*102A>C	NP_001293101.1:n.*102A>C
NR_037884.1:n.429-9215T>G
XR_938685.1:n.1584A>C
XR_938686.1:n.1575A>C
XR_938687.1:n.1448A>C
NM_000670.5:c.*102A>C MANE Select	NP_000661.2:n.*102A>C
NM_001306171.2:c.*102A>C	NP_001293100.1:n.*102A>C
NM_001306172.2:c.*102A>C	NP_001293101.1:n.*102A>C