Canonical Allele Identifier: CA357478573

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100045607T>A (hg19) ; chr4:g.99124456T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124456T>A , CM000666.2:g.99124456T>A	GRCh38
NC_000004.11:g.100045607T>A , CM000666.1:g.100045607T>A	GRCh37
NC_000004.10:g.100264630T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1129A>T MANE Select	ENSP00000265512.7:p.Ile377Phe
ENST00000265512.11:c.1129A>T	ENSP00000265512.7:p.Ile377Phe
ENST00000505590.5:c.1186A>T	ENSP00000425416.1:p.Ile396Phe
ENST00000508393.5:c.1186A>T	ENSP00000424630.1:p.Ile396Phe
ENST00000509471.5:c.483A>T	ENSP00000424583.1:n.483A>T
ENST00000629236.2:c.1129A>T	ENSP00000486450.1:p.Ile377Phe
NM_000670.3:c.1129A>T	NP_000661.2:p.Ile377Phe
NM_000670.4:c.1129A>T	NP_000661.2:p.Ile377Phe
NM_001306171.1:c.1186A>T	NP_001293100.1:p.Ile396Phe
NM_001306172.1:c.1186A>T	NP_001293101.1:p.Ile396Phe
NR_037884.1:n.429-9099T>A
XR_938685.1:n.1468A>T
XR_938686.1:n.1459A>T
XR_938687.1:n.1332A>T
NM_000670.5:c.1129A>T MANE Select	NP_000661.2:p.Ile377Phe
NM_001306171.2:c.1186A>T	NP_001293100.1:p.Ile396Phe
NM_001306172.2:c.1186A>T	NP_001293101.1:p.Ile396Phe