Canonical Allele Identifier: CA2361139813

Gene: AHCY

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34295408G= , CM000682.2:g.34295408G=	GRCh38
NC_000020.10:g.32883214G= , CM000682.1:g.32883214G=	GRCh37
NC_000020.9:g.32346875G=	NCBI36
NG_012630.1:g.21395C=
NG_012630.2:g.21395C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217426.7:c.206C= MANE Select	ENSP00000217426.2:p.Thr69=
ENST00000217426.6:c.206C=	ENSP00000217426.2:p.Thr69=
ENST00000468908.1:n.369C=
ENST00000480653.5:n.253C=
ENST00000538132.1:c.122C=	ENSP00000442820.1:p.Thr41=
ENST00000606061.1:n.293C=
NM_000687.2:c.206C=	NP_000678.1:p.Thr69=
NM_001161766.1:c.122C=	NP_001155238.1:p.Thr41=
XM_005260316.3:c.122C=	XP_005260373.1:p.Thr41=
XM_005260317.1:c.122C=	XP_005260374.1:p.Thr41=
XM_011528656.1:c.122C=	XP_011526958.1:p.Thr41=
XM_011528657.1:c.122C=	XP_011526959.1:p.Thr41=
XM_011528658.1:c.122C=	XP_011526960.1:p.Thr41=
XM_011528659.1:c.122C=	XP_011526961.1:p.Thr41=
XM_011528660.1:c.122C=	XP_011526962.1:p.Thr41=
NM_000687.3:c.206C=	NP_000678.1:p.Thr69=
NM_001322084.1:c.122C=	NP_001309013.1:p.Thr41=
NM_001322085.1:c.122C=	NP_001309014.1:p.Thr41=
NM_001322086.1:c.212C=	NP_001309015.1:p.Thr71=
NM_001362750.1:c.206C=	NP_001349679.1:p.Thr69=
XM_005260317.2:c.122C=	XP_005260374.1:p.Thr41=
XM_011528656.3:c.212C=	XP_011526958.2:p.Thr71=
XM_011528657.2:c.212C=	XP_011526959.2:p.Thr71=
XM_011528658.3:c.212C=	XP_011526960.2:p.Thr71=
XM_017027709.2:c.206C=	XP_016883198.1:p.Thr69=
XM_017027710.2:c.-219C=	XP_016883199.1:n.-219C=
NM_000687.4:c.206C= MANE Select	NP_000678.1:p.Thr69=
NM_001322084.2:c.122C=	NP_001309013.1:p.Thr41=
NM_001322085.2:c.122C=	NP_001309014.1:p.Thr41=
NM_001322086.2:c.212C=	NP_001309015.1:p.Thr71=
NM_001362750.2:c.206C=	NP_001349679.1:p.Thr69=
NM_001161766.2:c.122C=	NP_001155238.1:p.Thr41=