Canonical Allele Identifier: CA3018595

Gene: ADH4

Linked Data

• dbSNP Id: rs768031238
• ExAC: 4:100047742 T / C
• gnomAD v2: 4-100047742-T-C
• gnomAD v3: 4-99126591-T-C
• gnomAD v4: 4-99126591-T-C
• MyVariant Identifiers: chr4:g.100047742T>C (hg19) ; chr4:g.99126591T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126591T>C , CM000666.2:g.99126591T>C	GRCh38
NC_000004.11:g.100047742T>C , CM000666.1:g.100047742T>C	GRCh37
NC_000004.10:g.100266765T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+3A>G MANE Select	ENSP00000265512.7:n.1118+3A>G
ENST00000265512.11:c.1118+3A>G	ENSP00000265512.7:n.1118+3A>G
ENST00000505590.5:c.1175+3A>G	ENSP00000425416.1:n.1175+3A>G
ENST00000508393.5:c.1175+3A>G	ENSP00000424630.1:n.1175+3A>G
ENST00000509471.5:c.472+3A>G	ENSP00000424583.1:n.472+3A>G
ENST00000629236.2:c.1118+3A>G	ENSP00000486450.1:n.1118+3A>G
NM_000670.3:c.1118+3A>G	NP_000661.2:n.1118+3A>G
NM_000670.4:c.1118+3A>G	NP_000661.2:n.1118+3A>G
NM_001306171.1:c.1175+3A>G	NP_001293100.1:n.1175+3A>G
NM_001306172.1:c.1175+3A>G	NP_001293101.1:n.1175+3A>G
NR_037884.1:n.429-6964T>C
XR_938685.1:n.1346+3A>G
XR_938686.1:n.1337+3A>G
XR_938687.1:n.1210+3A>G
NM_000670.5:c.1118+3A>G MANE Select	NP_000661.2:n.1118+3A>G
NM_001306171.2:c.1175+3A>G	NP_001293100.1:n.1175+3A>G
NM_001306172.2:c.1175+3A>G	NP_001293101.1:n.1175+3A>G