Canonical Allele Identifier: CA440304151

Gene: ADH4

Linked Data

• dbSNP Id: rs1328156518
• gnomAD v2: 4-100047852-C-A
• gnomAD v4: 4-99126701-C-A
• MyVariant Identifiers: chr4:g.100047852C>A (hg19) ; chr4:g.99126701C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126701C>A , CM000666.2:g.99126701C>A	GRCh38
NC_000004.11:g.100047852C>A , CM000666.1:g.100047852C>A	GRCh37
NC_000004.10:g.100266875C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1011G>T MANE Select	ENSP00000265512.7:p.Leu337=
ENST00000265512.11:c.1011G>T	ENSP00000265512.7:p.Leu337=
ENST00000505590.5:c.1068G>T	ENSP00000425416.1:p.Leu356=
ENST00000506705.5:c.*985G>T	ENSP00000426667.1:n.*985G>T
ENST00000508393.5:c.1068G>T	ENSP00000424630.1:p.Leu356=
ENST00000509471.5:c.365G>T	ENSP00000424583.1:n.365G>T
ENST00000629236.2:c.1011G>T	ENSP00000486450.1:p.Leu337=
NM_000670.3:c.1011G>T	NP_000661.2:p.Leu337=
NM_000670.4:c.1011G>T	NP_000661.2:p.Leu337=
NM_001306171.1:c.1068G>T	NP_001293100.1:p.Leu356=
NM_001306172.1:c.1068G>T	NP_001293101.1:p.Leu356=
NR_037884.1:n.429-6854C>A
XR_938685.1:n.1239G>T
XR_938686.1:n.1230G>T
XR_938687.1:n.1103G>T
NM_000670.5:c.1011G>T MANE Select	NP_000661.2:p.Leu337=
NM_001306171.2:c.1068G>T	NP_001293100.1:p.Leu356=
NM_001306172.2:c.1068G>T	NP_001293101.1:p.Leu356=