Canonical Allele Identifier: CA2062160937

Gene: DAO

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.108894208A>T , CM000674.2:g.108894208A>T	GRCh38
NC_000012.11:g.109287984A>T , CM000674.1:g.109287984A>T	GRCh37
NC_000012.10:g.107812113A>T	NCBI36
NG_023236.1:g.19128A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228476.8:c.508-55A>T MANE Select	ENSP00000228476.3:n.508-55A>T
ENST00000228476.7:c.508-55A>T	ENSP00000228476.3:n.508-55A>T
ENST00000547122.5:c.*156-55A>T	ENSP00000448095.1:n.*156-55A>T
ENST00000547166.1:c.508-55A>T	ENSP00000447104.1:n.508-55A>T
ENST00000547768.5:c.139-55A>T	ENSP00000449967.1:n.139-55A>T
ENST00000549215.5:c.*59-55A>T	ENSP00000449248.1:n.*59-55A>T
ENST00000551281.5:c.310-55A>T	ENSP00000446853.1:n.310-55A>T
NM_001917.4:c.508-55A>T	NP_001908.3:n.508-55A>T
XM_005268692.2:c.442-55A>T	XP_005268749.1:n.442-55A>T
XM_011538004.1:c.508-55A>T	XP_011536306.1:n.508-55A>T
XM_011538005.1:c.508-55A>T	XP_011536307.1:n.508-55A>T
XM_005268692.4:c.442-55A>T	XP_005268749.1:n.442-55A>T
XM_011538004.2:c.508-55A>T	XP_011536306.1:n.508-55A>T
XM_011538005.2:c.508-55A>T	XP_011536307.1:n.508-55A>T
NM_001917.5:c.508-55A>T MANE Select	NP_001908.3:n.508-55A>T