Canonical Allele Identifier: CA357479399

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100047836T>A (hg19) ; chr4:g.99126685T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126685T>A , CM000666.2:g.99126685T>A	GRCh38
NC_000004.11:g.100047836T>A , CM000666.1:g.100047836T>A	GRCh37
NC_000004.10:g.100266859T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1027A>T MANE Select	ENSP00000265512.7:p.Asn343Tyr
ENST00000265512.11:c.1027A>T	ENSP00000265512.7:p.Asn343Tyr
ENST00000505590.5:c.1084A>T	ENSP00000425416.1:p.Asn362Tyr
ENST00000506705.5:c.*1001A>T	ENSP00000426667.1:n.*1001A>T
ENST00000508393.5:c.1084A>T	ENSP00000424630.1:p.Asn362Tyr
ENST00000509471.5:c.381A>T	ENSP00000424583.1:n.381A>T
ENST00000629236.2:c.1027A>T	ENSP00000486450.1:p.Asn343Tyr
NM_000670.3:c.1027A>T	NP_000661.2:p.Asn343Tyr
NM_000670.4:c.1027A>T	NP_000661.2:p.Asn343Tyr
NM_001306171.1:c.1084A>T	NP_001293100.1:p.Asn362Tyr
NM_001306172.1:c.1084A>T	NP_001293101.1:p.Asn362Tyr
NR_037884.1:n.429-6870T>A
XR_938685.1:n.1255A>T
XR_938686.1:n.1246A>T
XR_938687.1:n.1119A>T
NM_000670.5:c.1027A>T MANE Select	NP_000661.2:p.Asn343Tyr
NM_001306171.2:c.1084A>T	NP_001293100.1:p.Asn362Tyr
NM_001306172.2:c.1084A>T	NP_001293101.1:p.Asn362Tyr