Canonical Allele Identifier: CA473407249
Gene: ANO5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.22283757C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22262211C>A , CM000673.2:g.22262211C>A GRCh38
NC_000011.9:g.22283757C>A , CM000673.1:g.22283757C>A GRCh37
NC_000011.8:g.22240333C>A NCBI36
NG_015844.1:g.74036C>A , LRG_868:g.74036C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.1263C>A ENSP00000507766.1:p.Ser421=
ENST00000682341.1:c.1671C>A ENSP00000508251.1:p.Ser557=
ENST00000683197.1:c.1671C>A ENSP00000507641.1:p.Ser557=
ENST00000683411.1:c.1263C>A ENSP00000508397.1:p.Ser421=
ENST00000683437.1:c.1263C>A ENSP00000508408.1:p.Ser421=
ENST00000683613.1:n.2707C>A
ENST00000684663.1:c.1668C>A ENSP00000508009.1:p.Ser556=
ENST00000324559.9:c.1713C>A MANE Select ENSP00000315371.9:p.Ser571=
ENST00000648804.1:n.2048C>A
ENST00000324559.8:c.1713C>A ENSP00000315371.8:p.Ser571=
NM_001142649.1:c.1710C>A NP_001136121.1:p.Ser570=
NM_213599.2:c.1713C>A , LRG_868t1:c.1713C>A NP_998764.1:p.Ser571=
XM_005252820.2:c.1671C>A XP_005252877.2:p.Ser557=
XM_005252821.2:c.1668C>A XP_005252878.2:p.Ser556=
XM_005252822.3:c.1635C>A XP_005252879.1:p.Ser545=
XM_005252823.3:c.1632C>A XP_005252880.1:p.Ser544=
XM_011519949.1:c.1620C>A XP_011518251.1:p.Ser540=
XM_005252820.3:c.1671C>A XP_005252877.2:p.Ser557=
XM_005252821.3:c.1668C>A XP_005252878.2:p.Ser556=
XM_005252822.4:c.1635C>A XP_005252879.1:p.Ser545=
XM_011519949.2:c.1620C>A XP_011518251.1:p.Ser540=
NM_001142649.2:c.1710C>A NP_001136121.1:p.Ser570=
NM_213599.3:c.1713C>A MANE Select NP_998764.1:p.Ser571=