Canonical Allele Identifier: CA2361139859

Gene: AHCY

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34295482T= , CM000682.2:g.34295482T=	GRCh38
NC_000020.10:g.32883288T= , CM000682.1:g.32883288T=	GRCh37
NC_000020.9:g.32346949T=	NCBI36
NG_012630.1:g.21321A=
NG_012630.2:g.21321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217426.7:c.132A= MANE Select	ENSP00000217426.2:p.Pro44=
ENST00000217426.6:c.132A=	ENSP00000217426.2:p.Pro44=
ENST00000468908.1:n.295A=
ENST00000473516.1:n.435A=
ENST00000480653.5:n.179A=
ENST00000538132.1:c.48A=	ENSP00000442820.1:p.Pro16=
ENST00000606061.1:n.219A=
NM_000687.2:c.132A=	NP_000678.1:p.Pro44=
NM_001161766.1:c.48A=	NP_001155238.1:p.Pro16=
XM_005260316.3:c.48A=	XP_005260373.1:p.Pro16=
XM_005260317.1:c.48A=	XP_005260374.1:p.Pro16=
XM_011528656.1:c.48A=	XP_011526958.1:p.Pro16=
XM_011528657.1:c.48A=	XP_011526959.1:p.Pro16=
XM_011528658.1:c.48A=	XP_011526960.1:p.Pro16=
XM_011528659.1:c.48A=	XP_011526961.1:p.Pro16=
XM_011528660.1:c.48A=	XP_011526962.1:p.Pro16=
NM_000687.3:c.132A=	NP_000678.1:p.Pro44=
NM_001322084.1:c.48A=	NP_001309013.1:p.Pro16=
NM_001322085.1:c.48A=	NP_001309014.1:p.Pro16=
NM_001322086.1:c.138A=	NP_001309015.1:p.Pro46=
NM_001362750.1:c.132A=	NP_001349679.1:p.Pro44=
XM_005260317.2:c.48A=	XP_005260374.1:p.Pro16=
XM_011528656.3:c.138A=	XP_011526958.2:p.Pro46=
XM_011528657.2:c.138A=	XP_011526959.2:p.Pro46=
XM_011528658.3:c.138A=	XP_011526960.2:p.Pro46=
XM_017027709.2:c.132A=	XP_016883198.1:p.Pro44=
XM_017027710.2:c.-293A=	XP_016883199.1:n.-293A=
NM_000687.4:c.132A= MANE Select	NP_000678.1:p.Pro44=
NM_001322084.2:c.48A=	NP_001309013.1:p.Pro16=
NM_001322085.2:c.48A=	NP_001309014.1:p.Pro16=
NM_001322086.2:c.138A=	NP_001309015.1:p.Pro46=
NM_001362750.2:c.132A=	NP_001349679.1:p.Pro44=
NM_001161766.2:c.48A=	NP_001155238.1:p.Pro16=