Canonical Allele Identifier: CA357478568

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124455-A-G
• MyVariant Identifiers: chr4:g.100045606A>G (hg19) ; chr4:g.99124455A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124455A>G , CM000666.2:g.99124455A>G	GRCh38
NC_000004.11:g.100045606A>G , CM000666.1:g.100045606A>G	GRCh37
NC_000004.10:g.100264629A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1130T>C MANE Select	ENSP00000265512.7:p.Ile377Thr
ENST00000265512.11:c.1130T>C	ENSP00000265512.7:p.Ile377Thr
ENST00000505590.5:c.1187T>C	ENSP00000425416.1:p.Ile396Thr
ENST00000508393.5:c.1187T>C	ENSP00000424630.1:p.Ile396Thr
ENST00000509471.5:c.484T>C	ENSP00000424583.1:n.484T>C
ENST00000629236.2:c.1130T>C	ENSP00000486450.1:p.Ile377Thr
NM_000670.3:c.1130T>C	NP_000661.2:p.Ile377Thr
NM_000670.4:c.1130T>C	NP_000661.2:p.Ile377Thr
NM_001306171.1:c.1187T>C	NP_001293100.1:p.Ile396Thr
NM_001306172.1:c.1187T>C	NP_001293101.1:p.Ile396Thr
NR_037884.1:n.429-9100A>G
XR_938685.1:n.1469T>C
XR_938686.1:n.1460T>C
XR_938687.1:n.1333T>C
NM_000670.5:c.1130T>C MANE Select	NP_000661.2:p.Ile377Thr
NM_001306171.2:c.1187T>C	NP_001293100.1:p.Ile396Thr
NM_001306172.2:c.1187T>C	NP_001293101.1:p.Ile396Thr