Canonical Allele Identifier: CA357479455

Gene: ADH4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.1018G>T MANE Select	ENSP00000265512.7:p.Asp340Tyr
ENST00000265512.11:c.1018G>T	ENSP00000265512.7:p.Asp340Tyr
ENST00000505590.5:c.1075G>T	ENSP00000425416.1:p.Asp359Tyr
ENST00000506705.5:c.*992G>T	ENSP00000426667.1:n.*992G>T
ENST00000508393.5:c.1075G>T	ENSP00000424630.1:p.Asp359Tyr
ENST00000509471.5:c.372G>T	ENSP00000424583.1:n.372G>T
ENST00000629236.2:c.1018G>T	ENSP00000486450.1:p.Asp340Tyr
NM_000670.3:c.1018G>T	NP_000661.2:p.Asp340Tyr
NM_000670.4:c.1018G>T	NP_000661.2:p.Asp340Tyr
NM_001306171.1:c.1075G>T	NP_001293100.1:p.Asp359Tyr
NM_001306172.1:c.1075G>T	NP_001293101.1:p.Asp359Tyr
NR_037884.1:n.429-6861C>A
XR_938685.1:n.1246G>T
XR_938686.1:n.1237G>T
XR_938687.1:n.1110G>T
NM_000670.5:c.1018G>T MANE Select	NP_000661.2:p.Asp340Tyr
NM_001306171.2:c.1075G>T	NP_001293100.1:p.Asp359Tyr
NM_001306172.2:c.1075G>T	NP_001293101.1:p.Asp359Tyr