Canonical Allele Identifier: CA2671506621

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124407-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124407C>T , CM000666.2:g.99124407C>T	GRCh38
NC_000004.11:g.100045558C>T , CM000666.1:g.100045558C>T	GRCh37
NC_000004.10:g.100264581C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*35G>A MANE Select	ENSP00000265512.7:n.*35G>A
ENST00000265512.11:c.*35G>A	ENSP00000265512.7:n.*35G>A
ENST00000505590.5:c.*35G>A	ENSP00000425416.1:n.*35G>A
ENST00000508393.5:c.*35G>A	ENSP00000424630.1:n.*35G>A
ENST00000509471.5:c.532G>A	ENSP00000424583.1:n.532G>A
ENST00000629236.2:c.1175G>A	ENSP00000486450.1:p.Ter392=
NM_000670.3:c.*35G>A	NP_000661.2:n.*35G>A
NM_000670.4:c.*35G>A	NP_000661.2:n.*35G>A
NM_001306171.1:c.*35G>A	NP_001293100.1:n.*35G>A
NM_001306172.1:c.*35G>A	NP_001293101.1:n.*35G>A
NR_037884.1:n.429-9148C>T
XR_938685.1:n.1517G>A
XR_938686.1:n.1508G>A
XR_938687.1:n.1381G>A
NM_000670.5:c.*35G>A MANE Select	NP_000661.2:n.*35G>A
NM_001306171.2:c.*35G>A	NP_001293100.1:n.*35G>A
NM_001306172.2:c.*35G>A	NP_001293101.1:n.*35G>A