Canonical Allele Identifier: CA2652505254
Gene: AHCY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34295343G>T , CM000682.2:g.34295343G>T GRCh38
NC_000020.10:g.32883149G>T , CM000682.1:g.32883149G>T GRCh37
NC_000020.9:g.32346810G>T NCBI36
NG_012630.1:g.21460C>A
NG_012630.2:g.21460C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217426.7:c.219+52C>A MANE Select ENSP00000217426.2:n.219+52C>A
ENST00000217426.6:c.219+52C>A ENSP00000217426.2:n.219+52C>A
ENST00000468908.1:n.382+52C>A
ENST00000480653.5:n.266+52C>A
ENST00000538132.1:c.135+52C>A ENSP00000442820.1:n.135+52C>A
ENST00000606061.1:n.358C>A
NM_000687.2:c.219+52C>A NP_000678.1:n.219+52C>A
NM_001161766.1:c.135+52C>A NP_001155238.1:n.135+52C>A
XM_005260316.3:c.135+52C>A XP_005260373.1:n.135+52C>A
XM_005260317.1:c.135+52C>A XP_005260374.1:n.135+52C>A
XM_011528656.1:c.135+52C>A XP_011526958.1:n.135+52C>A
XM_011528657.1:c.135+52C>A XP_011526959.1:n.135+52C>A
XM_011528658.1:c.135+52C>A XP_011526960.1:n.135+52C>A
XM_011528659.1:c.135+52C>A XP_011526961.1:n.135+52C>A
XM_011528660.1:c.135+52C>A XP_011526962.1:n.135+52C>A
NM_000687.3:c.219+52C>A NP_000678.1:n.219+52C>A
NM_001322084.1:c.135+52C>A NP_001309013.1:n.135+52C>A
NM_001322085.1:c.135+52C>A NP_001309014.1:n.135+52C>A
NM_001322086.1:c.225+52C>A NP_001309015.1:n.225+52C>A
NM_001362750.1:c.219+52C>A NP_001349679.1:n.219+52C>A
XM_005260317.2:c.135+52C>A XP_005260374.1:n.135+52C>A
XM_011528656.3:c.225+52C>A XP_011526958.2:n.225+52C>A
XM_011528657.2:c.225+52C>A XP_011526959.2:n.225+52C>A
XM_011528658.3:c.225+52C>A XP_011526960.2:n.225+52C>A
XM_017027709.2:c.219+52C>A XP_016883198.1:n.219+52C>A
XM_017027710.2:c.-206+52C>A XP_016883199.1:n.-206+52C>A
NM_000687.4:c.219+52C>A MANE Select NP_000678.1:n.219+52C>A
NM_001322084.2:c.135+52C>A NP_001309013.1:n.135+52C>A
NM_001322085.2:c.135+52C>A NP_001309014.1:n.135+52C>A
NM_001322086.2:c.225+52C>A NP_001309015.1:n.225+52C>A
NM_001362750.2:c.219+52C>A NP_001349679.1:n.219+52C>A
NM_001161766.2:c.135+52C>A NP_001155238.1:n.135+52C>A