Canonical Allele Identifier: CA9821015
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs577419934

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34292381G>A , CM000682.2:g.34292381G>A GRCh38
NC_000020.10:g.32880187G>A , CM000682.1:g.32880187G>A GRCh37
NC_000020.9:g.32343848G>A NCBI36
NG_012630.1:g.24422C>T
NG_012630.2:g.24422C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000217426.7:c.422C>T MANE Select ENSP00000217426.2:p.Thr141Ile
ENST00000217426.6:c.422C>T ENSP00000217426.2:p.Thr141Ile
ENST00000468908.1:n.585C>T
ENST00000480653.5:n.469C>T
ENST00000538132.1:c.338C>T ENSP00000442820.1:p.Thr113Ile
NM_000687.2:c.422C>T NP_000678.1:p.Thr141Ile
NM_001161766.1:c.338C>T NP_001155238.1:p.Thr113Ile
XM_005260316.3:c.338C>T XP_005260373.1:p.Thr113Ile
XM_005260317.1:c.338C>T XP_005260374.1:p.Thr113Ile
XM_011528656.1:c.338C>T XP_011526958.1:p.Thr113Ile
XM_011528657.1:c.338C>T XP_011526959.1:p.Thr113Ile
XM_011528658.1:c.338C>T XP_011526960.1:p.Thr113Ile
XM_011528659.1:c.338C>T XP_011526961.1:p.Thr113Ile
XM_011528660.1:c.338C>T XP_011526962.1:p.Thr113Ile
NM_000687.3:c.422C>T NP_000678.1:p.Thr141Ile
NM_001322084.1:c.338C>T NP_001309013.1:p.Thr113Ile
NM_001322085.1:c.338C>T NP_001309014.1:p.Thr113Ile
NM_001322086.1:c.428C>T NP_001309015.1:p.Thr143Ile
NM_001362750.1:c.422C>T NP_001349679.1:p.Thr141Ile
XM_005260317.2:c.338C>T XP_005260374.1:p.Thr113Ile
XM_011528656.3:c.428C>T XP_011526958.2:p.Thr143Ile
XM_011528657.2:c.428C>T XP_011526959.2:p.Thr143Ile
XM_011528658.3:c.428C>T XP_011526960.2:p.Thr143Ile
XM_017027709.2:c.422C>T XP_016883198.1:p.Thr141Ile
XM_017027710.2:c.44C>T XP_016883199.1:p.Thr15Ile
NM_000687.4:c.422C>T MANE Select NP_000678.1:p.Thr141Ile
NM_001322084.2:c.338C>T NP_001309013.1:p.Thr113Ile
NM_001322085.2:c.338C>T NP_001309014.1:p.Thr113Ile
NM_001322086.2:c.428C>T NP_001309015.1:p.Thr143Ile
NM_001362750.2:c.422C>T NP_001349679.1:p.Thr141Ile
NM_001161766.2:c.338C>T NP_001155238.1:p.Thr113Ile