Canonical Allele Identifier: CA2361142784
Gene: AHCY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34301806G= , CM000682.2:g.34301806G= GRCh38
NC_000020.10:g.32889612G= , CM000682.1:g.32889612G= GRCh37
NC_000020.9:g.32353273G= NCBI36
NG_012630.1:g.14997C=
NG_012630.2:g.14997C=

Transcript Alleles

HGVS Amino-acid change
ENST00000217426.7:c.28+1437C= MANE Select ENSP00000217426.2:n.28+1437C=
ENST00000217426.6:c.28+1437C= ENSP00000217426.2:n.28+1437C=
ENST00000468908.1:n.143C=
ENST00000473516.1:n.331+539C=
ENST00000480653.5:n.75+1437C=
ENST00000538132.1:c.-56-6221C= ENSP00000442820.1:n.-56-6221C=
ENST00000606061.1:n.115+1437C=
NM_000687.2:c.28+1437C= NP_000678.1:n.28+1437C=
NM_001161766.1:c.-56-6221C= NP_001155238.1:n.-56-6221C=
XM_005260316.3:c.-105C= XP_005260373.1:n.-105C=
XM_005260317.1:c.-57+810C= XP_005260374.1:n.-57+810C=
XM_011528659.1:c.-56-6221C= XP_011526961.1:n.-56-6221C=
XM_011528660.1:c.-57+130C= XP_011526962.1:n.-57+130C=
NM_000687.3:c.28+1437C= NP_000678.1:n.28+1437C=
NM_001322084.1:c.-105C= NP_001309013.1:n.-105C=
NM_001322085.1:c.-57+130C= NP_001309014.1:n.-57+130C=
NM_001322086.1:c.-26C= NP_001309015.1:n.-26C=
NM_001362750.1:c.28+1437C= NP_001349679.1:n.28+1437C=
XM_005260317.2:c.-57+810C= XP_005260374.1:n.-57+810C=
XM_011528656.3:c.-26C= XP_011526958.2:n.-26C=
XM_011528657.2:c.-26C= XP_011526959.2:n.-26C=
XM_011528658.3:c.-26C= XP_011526960.2:n.-26C=
XM_017027709.2:c.28+1437C= XP_016883198.1:n.28+1437C=
XM_017027710.2:c.-397+1437C= XP_016883199.1:n.-397+1437C=
NM_000687.4:c.28+1437C= MANE Select NP_000678.1:n.28+1437C=
NM_001322084.2:c.-105C= NP_001309013.1:n.-105C=
NM_001322085.2:c.-57+130C= NP_001309014.1:n.-57+130C=
NM_001322086.2:c.-26C= NP_001309015.1:n.-26C=
NM_001362750.2:c.28+1437C= NP_001349679.1:n.28+1437C=
NM_001161766.2:c.-56-6221C= NP_001155238.1:n.-56-6221C=