Canonical Allele Identifier: CA357479456

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100047845C>G (hg19) ; chr4:g.99126694C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126694C>G , CM000666.2:g.99126694C>G	GRCh38
NC_000004.11:g.100047845C>G , CM000666.1:g.100047845C>G	GRCh37
NC_000004.10:g.100266868C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1018G>C MANE Select	ENSP00000265512.7:p.Asp340His
ENST00000265512.11:c.1018G>C	ENSP00000265512.7:p.Asp340His
ENST00000505590.5:c.1075G>C	ENSP00000425416.1:p.Asp359His
ENST00000506705.5:c.*992G>C	ENSP00000426667.1:n.*992G>C
ENST00000508393.5:c.1075G>C	ENSP00000424630.1:p.Asp359His
ENST00000509471.5:c.372G>C	ENSP00000424583.1:n.372G>C
ENST00000629236.2:c.1018G>C	ENSP00000486450.1:p.Asp340His
NM_000670.3:c.1018G>C	NP_000661.2:p.Asp340His
NM_000670.4:c.1018G>C	NP_000661.2:p.Asp340His
NM_001306171.1:c.1075G>C	NP_001293100.1:p.Asp359His
NM_001306172.1:c.1075G>C	NP_001293101.1:p.Asp359His
NR_037884.1:n.429-6861C>G
XR_938685.1:n.1246G>C
XR_938686.1:n.1237G>C
XR_938687.1:n.1110G>C
NM_000670.5:c.1018G>C MANE Select	NP_000661.2:p.Asp340His
NM_001306171.2:c.1075G>C	NP_001293100.1:p.Asp359His
NM_001306172.2:c.1075G>C	NP_001293101.1:p.Asp359His