Canonical Allele Identifier: CA379941945

Gene: ANO3

Linked Data

• ClinVar Variation Id: 455986
• ClinVar RCV Id: RCV000554751
• dbSNP Id: rs1554976233
• MyVariant Identifiers: chr11:g.26621232A>G (hg19) ; chr11:g.26599685A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.26599685A>G , CM000673.2:g.26599685A>G	GRCh38
NC_000011.9:g.26621232A>G , CM000673.1:g.26621232A>G	GRCh37
NC_000011.8:g.26577808A>G	NCBI36
NG_042856.1:g.415563A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000256737.8:c.1807A>G MANE Select	ENSP00000256737.3:p.Asn603Asp
ENST00000672621.1:c.1990A>G	ENSP00000500506.1:p.Asn664Asp
ENST00000256737.7:c.1807A>G	ENSP00000256737.3:p.Asn603Asp
ENST00000525139.5:c.1759A>G	ENSP00000432576.1:p.Asn587Asp
ENST00000531568.1:c.1369A>G	ENSP00000432394.1:p.Asn457Asp
NM_001313726.1:c.1990A>G	NP_001300655.1:p.Asn664Asp
NM_001313727.1:c.1369A>G	NP_001300656.1:p.Asn457Asp
NM_031418.2:c.1807A>G	NP_113606.2:p.Asn603Asp
NM_031418.3:c.1807A>G	NP_113606.2:p.Asn603Asp
XM_011520282.1:c.409A>G	XP_011518584.1:p.Asn137Asp
XM_011520282.3:c.409A>G	XP_011518584.1:p.Asn137Asp
XM_017018118.2:c.1369A>G	XP_016873607.1:p.Asn457Asp
XM_017018119.2:c.1078A>G	XP_016873608.1:p.Asn360Asp
NM_031418.4:c.1807A>G MANE Select	NP_113606.2:p.Asn603Asp
NM_001313726.2:c.1990A>G	NP_001300655.1:p.Asn664Asp
NM_001313727.2:c.1369A>G	NP_001300656.1:p.Asn457Asp