Canonical Allele Identifier: CA6525376
Gene: ANO6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45401980C>T , CM000674.2:g.45401980C>T GRCh38
NC_000012.11:g.45795763C>T , CM000674.1:g.45795763C>T GRCh37
NC_000012.10:g.44082030C>T NCBI36
NG_028220.1:g.190994C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320560.13:c.1572C>T MANE Select ENSP00000320087.8:p.Asn524=
ENST00000679426.1:c.1539C>T ENSP00000506600.1:p.Asn513=
ENST00000679761.1:c.1572C>T ENSP00000505361.1:p.Asn524=
ENST00000680201.1:c.1572C>T ENSP00000506222.1:p.Asn524=
ENST00000680371.1:c.1572C>T ENSP00000506392.1:p.Asn524=
ENST00000680498.1:c.1155C>T ENSP00000506613.1:p.Asn385=
ENST00000681156.1:c.1572C>T ENSP00000506069.1:p.Asn524=
ENST00000681817.1:c.1155C>T ENSP00000506683.1:p.Asn385=
ENST00000320560.12:c.1572C>T ENSP00000320087.8:p.Asn524=
ENST00000423947.7:c.1635C>T ENSP00000409126.3:p.Asn545=
ENST00000425752.6:c.1572C>T ENSP00000391417.2:p.Asn524=
ENST00000426898.2:n.1988C>T
ENST00000441606.2:c.1518C>T ENSP00000413137.2:p.Asn506=
NM_001025356.2:c.1572C>T NP_001020527.2:p.Asn524=
NM_001142678.1:c.1518C>T NP_001136150.1:p.Asn506=
NM_001142679.1:c.1572C>T NP_001136151.1:p.Asn524=
NM_001204803.1:c.1635C>T NP_001191732.1:p.Asn545=
XM_005268706.3:c.1539C>T XP_005268763.1:p.Asn513=
XM_005268707.2:c.1473C>T XP_005268764.1:p.Asn491=
XM_011538024.1:c.1635C>T XP_011536326.1:p.Asn545=
XR_944886.1:n.1352-3756G>A
XR_944888.1:n.1352-3756G>A
XM_005268706.5:c.1539C>T XP_005268763.1:p.Asn513=
XM_005268707.4:c.1473C>T XP_005268764.1:p.Asn491=
XR_001749096.1:n.1353-3756G>A
XR_944886.2:n.1353-3756G>A
NM_001025356.3:c.1572C>T MANE Select NP_001020527.2:p.Asn524=
NM_001142678.2:c.1518C>T NP_001136150.1:p.Asn506=
NM_001142679.2:c.1572C>T NP_001136151.1:p.Asn524=
NM_001204803.2:c.1635C>T NP_001191732.1:p.Asn545=