Canonical Allele Identifier: CA510273778

Gene: AHCY

Linked Data

• MyVariant Identifiers: chr20:g.32880192G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34292386G>A , CM000682.2:g.34292386G>A	GRCh38
NC_000020.10:g.32880192G>A , CM000682.1:g.32880192G>A	GRCh37
NC_000020.9:g.32343853G>A	NCBI36
NG_012630.1:g.24417C>T
NG_012630.2:g.24417C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217426.7:c.417C>T MANE Select	ENSP00000217426.2:p.Ile139=
ENST00000217426.6:c.417C>T	ENSP00000217426.2:p.Ile139=
ENST00000468908.1:n.580C>T
ENST00000480653.5:n.464C>T
ENST00000538132.1:c.333C>T	ENSP00000442820.1:p.Ile111=
NM_000687.2:c.417C>T	NP_000678.1:p.Ile139=
NM_001161766.1:c.333C>T	NP_001155238.1:p.Ile111=
XM_005260316.3:c.333C>T	XP_005260373.1:p.Ile111=
XM_005260317.1:c.333C>T	XP_005260374.1:p.Ile111=
XM_011528656.1:c.333C>T	XP_011526958.1:p.Ile111=
XM_011528657.1:c.333C>T	XP_011526959.1:p.Ile111=
XM_011528658.1:c.333C>T	XP_011526960.1:p.Ile111=
XM_011528659.1:c.333C>T	XP_011526961.1:p.Ile111=
XM_011528660.1:c.333C>T	XP_011526962.1:p.Ile111=
NM_000687.3:c.417C>T	NP_000678.1:p.Ile139=
NM_001322084.1:c.333C>T	NP_001309013.1:p.Ile111=
NM_001322085.1:c.333C>T	NP_001309014.1:p.Ile111=
NM_001322086.1:c.423C>T	NP_001309015.1:p.Ile141=
NM_001362750.1:c.417C>T	NP_001349679.1:p.Ile139=
XM_005260317.2:c.333C>T	XP_005260374.1:p.Ile111=
XM_011528656.3:c.423C>T	XP_011526958.2:p.Ile141=
XM_011528657.2:c.423C>T	XP_011526959.2:p.Ile141=
XM_011528658.3:c.423C>T	XP_011526960.2:p.Ile141=
XM_017027709.2:c.417C>T	XP_016883198.1:p.Ile139=
XM_017027710.2:c.39C>T	XP_016883199.1:p.Ile13=
NM_000687.4:c.417C>T MANE Select	NP_000678.1:p.Ile139=
NM_001322084.2:c.333C>T	NP_001309013.1:p.Ile111=
NM_001322085.2:c.333C>T	NP_001309014.1:p.Ile111=
NM_001322086.2:c.423C>T	NP_001309015.1:p.Ile141=
NM_001362750.2:c.417C>T	NP_001349679.1:p.Ile139=
NM_001161766.2:c.333C>T	NP_001155238.1:p.Ile111=