Canonical Allele Identifier: CA2361139879
Gene: AHCY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34295517T= , CM000682.2:g.34295517T= GRCh38
NC_000020.10:g.32883323T= , CM000682.1:g.32883323T= GRCh37
NC_000020.9:g.32346984T= NCBI36
NG_012630.1:g.21286A=
NG_012630.2:g.21286A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217426.7:c.97A= MANE Select ENSP00000217426.2:p.Met33=
ENST00000217426.6:c.97A= ENSP00000217426.2:p.Met33=
ENST00000468908.1:n.260A=
ENST00000473516.1:n.400A=
ENST00000480653.5:n.144A=
ENST00000538132.1:c.13A= ENSP00000442820.1:p.Met5=
ENST00000606061.1:n.184A=
NM_000687.2:c.97A= NP_000678.1:p.Met33=
NM_001161766.1:c.13A= NP_001155238.1:p.Met5=
XM_005260316.3:c.13A= XP_005260373.1:p.Met5=
XM_005260317.1:c.13A= XP_005260374.1:p.Met5=
XM_011528656.1:c.13A= XP_011526958.1:p.Met5=
XM_011528657.1:c.13A= XP_011526959.1:p.Met5=
XM_011528658.1:c.13A= XP_011526960.1:p.Met5=
XM_011528659.1:c.13A= XP_011526961.1:p.Met5=
XM_011528660.1:c.13A= XP_011526962.1:p.Met5=
NM_000687.3:c.97A= NP_000678.1:p.Met33=
NM_001322084.1:c.13A= NP_001309013.1:p.Met5=
NM_001322085.1:c.13A= NP_001309014.1:p.Met5=
NM_001322086.1:c.103A= NP_001309015.1:p.Met35=
NM_001362750.1:c.97A= NP_001349679.1:p.Met33=
XM_005260317.2:c.13A= XP_005260374.1:p.Met5=
XM_011528656.3:c.103A= XP_011526958.2:p.Met35=
XM_011528657.2:c.103A= XP_011526959.2:p.Met35=
XM_011528658.3:c.103A= XP_011526960.2:p.Met35=
XM_017027709.2:c.97A= XP_016883198.1:p.Met33=
XM_017027710.2:c.-328A= XP_016883199.1:n.-328A=
NM_000687.4:c.97A= MANE Select NP_000678.1:p.Met33=
NM_001322084.2:c.13A= NP_001309013.1:p.Met5=
NM_001322085.2:c.13A= NP_001309014.1:p.Met5=
NM_001322086.2:c.103A= NP_001309015.1:p.Met35=
NM_001362750.2:c.97A= NP_001349679.1:p.Met33=
NM_001161766.2:c.13A= NP_001155238.1:p.Met5=