Canonical Allele Identifier: CA2361135335

Gene: AHCY

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34285813G>T , CM000682.2:g.34285813G>T	GRCh38
NC_000020.10:g.32873619G>T , CM000682.1:g.32873619G>T	GRCh37
NC_000020.9:g.32337280G>T	NCBI36
NG_012630.1:g.30990C>A
NG_012630.2:g.30990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217426.7:c.973-179C>A MANE Select	ENSP00000217426.2:n.973-179C>A
ENST00000217426.6:c.973-179C>A	ENSP00000217426.2:n.973-179C>A
ENST00000480653.5:n.1121-179C>A
ENST00000538132.1:c.889-179C>A	ENSP00000442820.1:n.889-179C>A
NM_000687.2:c.973-179C>A	NP_000678.1:n.973-179C>A
NM_001161766.1:c.889-179C>A	NP_001155238.1:n.889-179C>A
XM_005260316.3:c.889-179C>A	XP_005260373.1:n.889-179C>A
XM_005260317.1:c.889-179C>A	XP_005260374.1:n.889-179C>A
XM_011528656.1:c.889-179C>A	XP_011526958.1:n.889-179C>A
XM_011528657.1:c.889-179C>A	XP_011526959.1:n.889-179C>A
XM_011528658.1:c.889-179C>A	XP_011526960.1:n.889-179C>A
XM_011528659.1:c.889-179C>A	XP_011526961.1:n.889-179C>A
XM_011528660.1:c.889-179C>A	XP_011526962.1:n.889-179C>A
NM_000687.3:c.973-179C>A	NP_000678.1:n.973-179C>A
NM_001322084.1:c.889-179C>A	NP_001309013.1:n.889-179C>A
NM_001322085.1:c.889-179C>A	NP_001309014.1:n.889-179C>A
NM_001322086.1:c.979-179C>A	NP_001309015.1:n.979-179C>A
NM_001362750.1:c.973-179C>A	NP_001349679.1:n.973-179C>A
XM_005260317.2:c.889-179C>A	XP_005260374.1:n.889-179C>A
XM_011528656.3:c.979-179C>A	XP_011526958.2:n.979-179C>A
XM_011528657.2:c.979-179C>A	XP_011526959.2:n.979-179C>A
XM_011528658.3:c.979-179C>A	XP_011526960.2:n.979-179C>A
XM_017027709.2:c.973-179C>A	XP_016883198.1:n.973-179C>A
XM_017027710.2:c.595-179C>A	XP_016883199.1:n.595-179C>A
NM_000687.4:c.973-179C>A MANE Select	NP_000678.1:n.973-179C>A
NM_001322084.2:c.889-179C>A	NP_001309013.1:n.889-179C>A
NM_001322085.2:c.889-179C>A	NP_001309014.1:n.889-179C>A
NM_001322086.2:c.979-179C>A	NP_001309015.1:n.979-179C>A
NM_001362750.2:c.973-179C>A	NP_001349679.1:n.973-179C>A
NM_001161766.2:c.889-179C>A	NP_001155238.1:n.889-179C>A