Canonical Allele Identifier: CA357478257

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100045573C>T (hg19) ; chr4:g.99124422C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124422C>T , CM000666.2:g.99124422C>T	GRCh38
NC_000004.11:g.100045573C>T , CM000666.1:g.100045573C>T	GRCh37
NC_000004.10:g.100264596C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*20G>A MANE Select	ENSP00000265512.7:n.*20G>A
ENST00000265512.11:c.*20G>A	ENSP00000265512.7:n.*20G>A
ENST00000505590.5:c.*20G>A	ENSP00000425416.1:n.*20G>A
ENST00000508393.5:c.*20G>A	ENSP00000424630.1:n.*20G>A
ENST00000509471.5:c.517G>A	ENSP00000424583.1:n.517G>A
ENST00000629236.2:c.1160G>A	ENSP00000486450.1:p.Arg387Lys
NM_000670.3:c.*20G>A	NP_000661.2:n.*20G>A
NM_000670.4:c.*20G>A	NP_000661.2:n.*20G>A
NM_001306171.1:c.*20G>A	NP_001293100.1:n.*20G>A
NM_001306172.1:c.*20G>A	NP_001293101.1:n.*20G>A
NR_037884.1:n.429-9133C>T
XR_938685.1:n.1502G>A
XR_938686.1:n.1493G>A
XR_938687.1:n.1366G>A
NM_000670.5:c.*20G>A MANE Select	NP_000661.2:n.*20G>A
NM_001306171.2:c.*20G>A	NP_001293100.1:n.*20G>A
NM_001306172.2:c.*20G>A	NP_001293101.1:n.*20G>A