Canonical Allele Identifier: CA440304942

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048421T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127270T>A , CM000666.2:g.99127270T>A	GRCh38
NC_000004.11:g.100048421T>A , CM000666.1:g.100048421T>A	GRCh37
NC_000004.10:g.100267444T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.918A>T MANE Select	ENSP00000265512.7:p.Gly306=
ENST00000265512.11:c.918A>T	ENSP00000265512.7:p.Gly306=
ENST00000505590.5:c.975A>T	ENSP00000425416.1:p.Gly325=
ENST00000506705.5:c.*892A>T	ENSP00000426667.1:n.*892A>T
ENST00000508393.5:c.975A>T	ENSP00000424630.1:p.Gly325=
ENST00000509471.5:c.334-538A>T	ENSP00000424583.1:n.334-538A>T
ENST00000629236.2:c.918A>T	ENSP00000486450.1:p.Gly306=
NM_000670.3:c.918A>T	NP_000661.2:p.Gly306=
NM_000670.4:c.918A>T	NP_000661.2:p.Gly306=
NM_001306171.1:c.975A>T	NP_001293100.1:p.Gly325=
NM_001306172.1:c.975A>T	NP_001293101.1:p.Gly325=
NR_037884.1:n.429-6285T>A
XR_938685.1:n.1146A>T
XR_938686.1:n.1137A>T
XR_938687.1:n.1010A>T
NM_000670.5:c.918A>T MANE Select	NP_000661.2:p.Gly306=
NM_001306171.2:c.975A>T	NP_001293100.1:p.Gly325=
NM_001306172.2:c.975A>T	NP_001293101.1:p.Gly325=