Canonical Allele Identifier: CA101601014

Gene: ADH4

Linked Data

• dbSNP Id: rs557014519
• gnomAD v4: 4-99124679-G-C
• MyVariant Identifiers: chr4:g.100045830G>C (hg19) ; chr4:g.99124679G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124679G>C , CM000666.2:g.99124679G>C	GRCh38
NC_000004.11:g.100045830G>C , CM000666.1:g.100045830G>C	GRCh37
NC_000004.10:g.100264853G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1119-213C>G MANE Select	ENSP00000265512.7:n.1119-213C>G
ENST00000265512.11:c.1119-213C>G	ENSP00000265512.7:n.1119-213C>G
ENST00000505590.5:c.1176-213C>G	ENSP00000425416.1:n.1176-213C>G
ENST00000508393.5:c.1176-213C>G	ENSP00000424630.1:n.1176-213C>G
ENST00000509471.5:c.473-213C>G	ENSP00000424583.1:n.473-213C>G
ENST00000629236.2:c.1119-213C>G	ENSP00000486450.1:n.1119-213C>G
NM_000670.3:c.1119-213C>G	NP_000661.2:n.1119-213C>G
NM_000670.4:c.1119-213C>G	NP_000661.2:n.1119-213C>G
NM_001306171.1:c.1176-213C>G	NP_001293100.1:n.1176-213C>G
NM_001306172.1:c.1176-213C>G	NP_001293101.1:n.1176-213C>G
NR_037884.1:n.429-8876G>C
XR_938685.1:n.1457+13C>G
XR_938686.1:n.1448+13C>G
XR_938687.1:n.1321+13C>G
NM_000670.5:c.1119-213C>G MANE Select	NP_000661.2:n.1119-213C>G
NM_001306171.2:c.1176-213C>G	NP_001293100.1:n.1176-213C>G
NM_001306172.2:c.1176-213C>G	NP_001293101.1:n.1176-213C>G