Canonical Allele Identifier: CA2361138429

Gene: AHCY

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34292387A= , CM000682.2:g.34292387A=	GRCh38
NC_000020.10:g.32880193A= , CM000682.1:g.32880193A=	GRCh37
NC_000020.9:g.32343854A=	NCBI36
NG_012630.1:g.24416T=
NG_012630.2:g.24416T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217426.7:c.416T= MANE Select	ENSP00000217426.2:p.Ile139=
ENST00000217426.6:c.416T=	ENSP00000217426.2:p.Ile139=
ENST00000468908.1:n.579T=
ENST00000480653.5:n.463T=
ENST00000538132.1:c.332T=	ENSP00000442820.1:p.Ile111=
NM_000687.2:c.416T=	NP_000678.1:p.Ile139=
NM_001161766.1:c.332T=	NP_001155238.1:p.Ile111=
XM_005260316.3:c.332T=	XP_005260373.1:p.Ile111=
XM_005260317.1:c.332T=	XP_005260374.1:p.Ile111=
XM_011528656.1:c.332T=	XP_011526958.1:p.Ile111=
XM_011528657.1:c.332T=	XP_011526959.1:p.Ile111=
XM_011528658.1:c.332T=	XP_011526960.1:p.Ile111=
XM_011528659.1:c.332T=	XP_011526961.1:p.Ile111=
XM_011528660.1:c.332T=	XP_011526962.1:p.Ile111=
NM_000687.3:c.416T=	NP_000678.1:p.Ile139=
NM_001322084.1:c.332T=	NP_001309013.1:p.Ile111=
NM_001322085.1:c.332T=	NP_001309014.1:p.Ile111=
NM_001322086.1:c.422T=	NP_001309015.1:p.Ile141=
NM_001362750.1:c.416T=	NP_001349679.1:p.Ile139=
XM_005260317.2:c.332T=	XP_005260374.1:p.Ile111=
XM_011528656.3:c.422T=	XP_011526958.2:p.Ile141=
XM_011528657.2:c.422T=	XP_011526959.2:p.Ile141=
XM_011528658.3:c.422T=	XP_011526960.2:p.Ile141=
XM_017027709.2:c.416T=	XP_016883198.1:p.Ile139=
XM_017027710.2:c.38T=	XP_016883199.1:p.Ile13=
NM_000687.4:c.416T= MANE Select	NP_000678.1:p.Ile139=
NM_001322084.2:c.332T=	NP_001309013.1:p.Ile111=
NM_001322085.2:c.332T=	NP_001309014.1:p.Ile111=
NM_001322086.2:c.422T=	NP_001309015.1:p.Ile141=
NM_001362750.2:c.416T=	NP_001349679.1:p.Ile139=
NM_001161766.2:c.332T=	NP_001155238.1:p.Ile111=