Canonical Allele Identifier: CA2361138375
Gene: AHCY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34292276T= , CM000682.2:g.34292276T= GRCh38
NC_000020.10:g.32880082T= , CM000682.1:g.32880082T= GRCh37
NC_000020.9:g.32343743T= NCBI36
NG_012630.1:g.24527A=
NG_012630.2:g.24527A=

Transcript Alleles

HGVS Amino-acid change
ENST00000217426.7:c.445+82A= MANE Select ENSP00000217426.2:n.445+82A=
ENST00000217426.6:c.445+82A= ENSP00000217426.2:n.445+82A=
ENST00000468908.1:n.608+82A=
ENST00000480653.5:n.492+82A=
ENST00000538132.1:c.361+82A= ENSP00000442820.1:n.361+82A=
NM_000687.2:c.445+82A= NP_000678.1:n.445+82A=
NM_001161766.1:c.361+82A= NP_001155238.1:n.361+82A=
XM_005260316.3:c.361+82A= XP_005260373.1:n.361+82A=
XM_005260317.1:c.361+82A= XP_005260374.1:n.361+82A=
XM_011528656.1:c.361+82A= XP_011526958.1:n.361+82A=
XM_011528657.1:c.361+82A= XP_011526959.1:n.361+82A=
XM_011528658.1:c.361+82A= XP_011526960.1:n.361+82A=
XM_011528659.1:c.361+82A= XP_011526961.1:n.361+82A=
XM_011528660.1:c.361+82A= XP_011526962.1:n.361+82A=
NM_000687.3:c.445+82A= NP_000678.1:n.445+82A=
NM_001322084.1:c.361+82A= NP_001309013.1:n.361+82A=
NM_001322085.1:c.361+82A= NP_001309014.1:n.361+82A=
NM_001322086.1:c.451+82A= NP_001309015.1:n.451+82A=
NM_001362750.1:c.445+82A= NP_001349679.1:n.445+82A=
XM_005260317.2:c.361+82A= XP_005260374.1:n.361+82A=
XM_011528656.3:c.451+82A= XP_011526958.2:n.451+82A=
XM_011528657.2:c.451+82A= XP_011526959.2:n.451+82A=
XM_011528658.3:c.451+82A= XP_011526960.2:n.451+82A=
XM_017027709.2:c.445+82A= XP_016883198.1:n.445+82A=
XM_017027710.2:c.67+82A= XP_016883199.1:n.67+82A=
NM_000687.4:c.445+82A= MANE Select NP_000678.1:n.445+82A=
NM_001322084.2:c.361+82A= NP_001309013.1:n.361+82A=
NM_001322085.2:c.361+82A= NP_001309014.1:n.361+82A=
NM_001322086.2:c.451+82A= NP_001309015.1:n.451+82A=
NM_001362750.2:c.445+82A= NP_001349679.1:n.445+82A=
NM_001161766.2:c.361+82A= NP_001155238.1:n.361+82A=