Canonical Allele Identifier: CA357478562

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124453-G-A
• MyVariant Identifiers: chr4:g.100045604G>A (hg19) ; chr4:g.99124453G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124453G>A , CM000666.2:g.99124453G>A	GRCh38
NC_000004.11:g.100045604G>A , CM000666.1:g.100045604G>A	GRCh37
NC_000004.10:g.100264627G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1132C>T MANE Select	ENSP00000265512.7:p.Leu378Phe
ENST00000265512.11:c.1132C>T	ENSP00000265512.7:p.Leu378Phe
ENST00000505590.5:c.1189C>T	ENSP00000425416.1:p.Leu397Phe
ENST00000508393.5:c.1189C>T	ENSP00000424630.1:p.Leu397Phe
ENST00000509471.5:c.486C>T	ENSP00000424583.1:n.486C>T
ENST00000629236.2:c.1132C>T	ENSP00000486450.1:p.Leu378Phe
NM_000670.3:c.1132C>T	NP_000661.2:p.Leu378Phe
NM_000670.4:c.1132C>T	NP_000661.2:p.Leu378Phe
NM_001306171.1:c.1189C>T	NP_001293100.1:p.Leu397Phe
NM_001306172.1:c.1189C>T	NP_001293101.1:p.Leu397Phe
NR_037884.1:n.429-9102G>A
XR_938685.1:n.1471C>T
XR_938686.1:n.1462C>T
XR_938687.1:n.1335C>T
NM_000670.5:c.1132C>T MANE Select	NP_000661.2:p.Leu378Phe
NM_001306171.2:c.1189C>T	NP_001293100.1:p.Leu397Phe
NM_001306172.2:c.1189C>T	NP_001293101.1:p.Leu397Phe