Canonical Allele Identifier: CA2577375328

Gene: AHCY

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34301826C>G , CM000682.2:g.34301826C>G	GRCh38
NC_000020.10:g.32889632C>G , CM000682.1:g.32889632C>G	GRCh37
NC_000020.9:g.32353293C>G	NCBI36
NG_012630.1:g.14977G>C
NG_012630.2:g.14977G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000217426.7:c.28+1417G>C MANE Select	ENSP00000217426.2:n.28+1417G>C
ENST00000217426.6:c.28+1417G>C	ENSP00000217426.2:n.28+1417G>C
ENST00000468908.1:n.123G>C
ENST00000473516.1:n.331+519G>C
ENST00000480653.5:n.75+1417G>C
ENST00000538132.1:c.-56-6241G>C	ENSP00000442820.1:n.-56-6241G>C
ENST00000606061.1:n.115+1417G>C
NM_000687.2:c.28+1417G>C	NP_000678.1:n.28+1417G>C
NM_001161766.1:c.-56-6241G>C	NP_001155238.1:n.-56-6241G>C
XM_005260316.3:c.-125G>C	XP_005260373.1:n.-125G>C
XM_005260317.1:c.-57+790G>C	XP_005260374.1:n.-57+790G>C
XM_011528659.1:c.-56-6241G>C	XP_011526961.1:n.-56-6241G>C
XM_011528660.1:c.-57+110G>C	XP_011526962.1:n.-57+110G>C
NM_000687.3:c.28+1417G>C	NP_000678.1:n.28+1417G>C
NM_001322084.1:c.-125G>C	NP_001309013.1:n.-125G>C
NM_001322085.1:c.-57+110G>C	NP_001309014.1:n.-57+110G>C
NM_001322086.1:c.-46G>C	NP_001309015.1:n.-46G>C
NM_001362750.1:c.28+1417G>C	NP_001349679.1:n.28+1417G>C
XM_005260317.2:c.-57+790G>C	XP_005260374.1:n.-57+790G>C
XM_011528656.3:c.-46G>C	XP_011526958.2:n.-46G>C
XM_011528657.2:c.-46G>C	XP_011526959.2:n.-46G>C
XM_011528658.3:c.-46G>C	XP_011526960.2:n.-46G>C
XM_017027709.2:c.28+1417G>C	XP_016883198.1:n.28+1417G>C
XM_017027710.2:c.-397+1417G>C	XP_016883199.1:n.-397+1417G>C
NM_000687.4:c.28+1417G>C MANE Select	NP_000678.1:n.28+1417G>C
NM_001322084.2:c.-125G>C	NP_001309013.1:n.-125G>C
NM_001322085.2:c.-57+110G>C	NP_001309014.1:n.-57+110G>C
NM_001322086.2:c.-46G>C	NP_001309015.1:n.-46G>C
NM_001362750.2:c.28+1417G>C	NP_001349679.1:n.28+1417G>C
NM_001161766.2:c.-56-6241G>C	NP_001155238.1:n.-56-6241G>C