Canonical Allele Identifier: CA1479867804

Gene: ADH4

Linked Data

• dbSNP Id: rs1729732833
• gnomAD v4: 4-99144275-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99144275A>G , CM000666.2:g.99144275A>G	GRCh38
NC_000004.11:g.100065426A>G , CM000666.1:g.100065426A>G	GRCh37
NC_000004.10:g.100284449A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.-53T>C MANE Select	ENSP00000265512.7:n.-53T>C
ENST00000265512.11:c.-53T>C	ENSP00000265512.7:n.-53T>C
ENST00000504581.1:n.170-1495T>C
ENST00000504894.1:c.-114T>C	ENSP00000427261.1:n.-114T>C
ENST00000505590.5:c.-136T>C	ENSP00000425416.1:n.-136T>C
ENST00000506705.5:c.-136T>C	ENSP00000426667.1:n.-136T>C
ENST00000508393.5:c.-144T>C	ENSP00000424630.1:n.-144T>C
ENST00000629236.2:c.-53T>C	ENSP00000486450.1:n.-53T>C
NM_000670.3:c.-53T>C	NP_000661.2:n.-53T>C
NM_000670.4:c.-53T>C	NP_000661.2:n.-53T>C
NM_001306171.1:c.-144T>C	NP_001293100.1:n.-144T>C
NM_001306172.1:c.-136T>C	NP_001293101.1:n.-136T>C
NR_037884.1:n.680-10270A>G
XR_938685.1:n.36T>C
XR_938686.1:n.19T>C
XR_938687.1:n.40T>C
NM_000670.5:c.-53T>C MANE Select	NP_000661.2:n.-53T>C
NM_001306171.2:c.-144T>C	NP_001293100.1:n.-144T>C
NM_001306172.2:c.-136T>C	NP_001293101.1:n.-136T>C