Canonical Allele Identifier: CA101600953

Gene: ADH4

Linked Data

• dbSNP Id: rs534936063
• gnomAD v2: 4-100045686-G-A
• gnomAD v3: 4-99124535-G-A
• gnomAD v4: 4-99124535-G-A
• MyVariant Identifiers: chr4:g.100045686G>A (hg19) ; chr4:g.99124535G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124535G>A , CM000666.2:g.99124535G>A	GRCh38
NC_000004.11:g.100045686G>A , CM000666.1:g.100045686G>A	GRCh37
NC_000004.10:g.100264709G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1119-69C>T MANE Select	ENSP00000265512.7:n.1119-69C>T
ENST00000265512.11:c.1119-69C>T	ENSP00000265512.7:n.1119-69C>T
ENST00000505590.5:c.1176-69C>T	ENSP00000425416.1:n.1176-69C>T
ENST00000508393.5:c.1176-69C>T	ENSP00000424630.1:n.1176-69C>T
ENST00000509471.5:c.473-69C>T	ENSP00000424583.1:n.473-69C>T
ENST00000629236.2:c.1119-69C>T	ENSP00000486450.1:n.1119-69C>T
NM_000670.3:c.1119-69C>T	NP_000661.2:n.1119-69C>T
NM_000670.4:c.1119-69C>T	NP_000661.2:n.1119-69C>T
NM_001306171.1:c.1176-69C>T	NP_001293100.1:n.1176-69C>T
NM_001306172.1:c.1176-69C>T	NP_001293101.1:n.1176-69C>T
NR_037884.1:n.429-9020G>A
XR_938685.1:n.1458-69C>T
XR_938686.1:n.1449-69C>T
XR_938687.1:n.1322-69C>T
NM_000670.5:c.1119-69C>T MANE Select	NP_000661.2:n.1119-69C>T
NM_001306171.2:c.1176-69C>T	NP_001293100.1:n.1176-69C>T
NM_001306172.2:c.1176-69C>T	NP_001293101.1:n.1176-69C>T