Canonical Allele Identifier: CA3018668

Gene: ADH4

Linked Data

• dbSNP Id: rs200208857
• ExAC: 4:100048471 C / T
• gnomAD v2: 4-100048471-C-T
• gnomAD v3: 4-99127320-C-T
• gnomAD v4: 4-99127320-C-T
• MyVariant Identifiers: chr4:g.100048471C>T (hg19) ; chr4:g.99127320C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127320C>T , CM000666.2:g.99127320C>T	GRCh38
NC_000004.11:g.100048471C>T , CM000666.1:g.100048471C>T	GRCh37
NC_000004.10:g.100267494C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.868G>A MANE Select	ENSP00000265512.7:p.Ala290Thr
ENST00000265512.11:c.868G>A	ENSP00000265512.7:p.Ala290Thr
ENST00000505590.5:c.925G>A	ENSP00000425416.1:p.Ala309Thr
ENST00000506705.5:c.*842G>A	ENSP00000426667.1:n.*842G>A
ENST00000508393.5:c.925G>A	ENSP00000424630.1:p.Ala309Thr
ENST00000509471.5:c.334-588G>A	ENSP00000424583.1:n.334-588G>A
ENST00000629236.2:c.868G>A	ENSP00000486450.1:p.Ala290Thr
NM_000670.3:c.868G>A	NP_000661.2:p.Ala290Thr
NM_000670.4:c.868G>A	NP_000661.2:p.Ala290Thr
NM_001306171.1:c.925G>A	NP_001293100.1:p.Ala309Thr
NM_001306172.1:c.925G>A	NP_001293101.1:p.Ala309Thr
NR_037884.1:n.429-6235C>T
XR_938685.1:n.1096G>A
XR_938686.1:n.1087G>A
XR_938687.1:n.960G>A
NM_000670.5:c.868G>A MANE Select	NP_000661.2:p.Ala290Thr
NM_001306171.2:c.925G>A	NP_001293100.1:p.Ala309Thr
NM_001306172.2:c.925G>A	NP_001293101.1:p.Ala309Thr