Canonical Allele Identifier: CA357478198

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100045565A>T (hg19) ; chr4:g.99124414A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124414A>T , CM000666.2:g.99124414A>T	GRCh38
NC_000004.11:g.100045565A>T , CM000666.1:g.100045565A>T	GRCh37
NC_000004.10:g.100264588A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*28T>A MANE Select	ENSP00000265512.7:n.*28T>A
ENST00000265512.11:c.*28T>A	ENSP00000265512.7:n.*28T>A
ENST00000505590.5:c.*28T>A	ENSP00000425416.1:n.*28T>A
ENST00000508393.5:c.*28T>A	ENSP00000424630.1:n.*28T>A
ENST00000509471.5:c.525T>A	ENSP00000424583.1:n.525T>A
ENST00000629236.2:c.1168T>A	ENSP00000486450.1:p.Ser390Thr
NM_000670.3:c.*28T>A	NP_000661.2:n.*28T>A
NM_000670.4:c.*28T>A	NP_000661.2:n.*28T>A
NM_001306171.1:c.*28T>A	NP_001293100.1:n.*28T>A
NM_001306172.1:c.*28T>A	NP_001293101.1:n.*28T>A
NR_037884.1:n.429-9141A>T
XR_938685.1:n.1510T>A
XR_938686.1:n.1501T>A
XR_938687.1:n.1374T>A
NM_000670.5:c.*28T>A MANE Select	NP_000661.2:n.*28T>A
NM_001306171.2:c.*28T>A	NP_001293100.1:n.*28T>A
NM_001306172.2:c.*28T>A	NP_001293101.1:n.*28T>A