Canonical Allele Identifier: CA6525503

Gene: ANO6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45416715C>T , CM000674.2:g.45416715C>T	GRCh38
NC_000012.11:g.45810498C>T , CM000674.1:g.45810498C>T	GRCh37
NC_000012.10:g.44096765C>T	NCBI36
NG_028220.1:g.205729C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320560.13:c.2028C>T MANE Select	ENSP00000320087.8:p.Phe676=
ENST00000679426.1:c.1995C>T	ENSP00000506600.1:p.Phe665=
ENST00000679761.1:c.2012-4356C>T	ENSP00000505361.1:n.2012-4356C>T
ENST00000680201.1:c.2028C>T	ENSP00000506222.1:p.Phe676=
ENST00000680371.1:c.*36-74C>T	ENSP00000506392.1:n.*36-74C>T
ENST00000680498.1:c.1611C>T	ENSP00000506613.1:p.Phe537=
ENST00000681156.1:c.2028C>T	ENSP00000506069.1:p.Phe676=
ENST00000681817.1:c.1611C>T	ENSP00000506683.1:p.Phe537=
ENST00000320560.12:c.2028C>T	ENSP00000320087.8:p.Phe676=
ENST00000423947.7:c.2091C>T	ENSP00000409126.3:p.Phe697=
ENST00000425752.6:c.2028C>T	ENSP00000391417.2:p.Phe676=
ENST00000426898.2:n.2444C>T
ENST00000441606.2:c.1974C>T	ENSP00000413137.2:p.Phe658=
NM_001025356.2:c.2028C>T	NP_001020527.2:p.Phe676=
NM_001142678.1:c.1974C>T	NP_001136150.1:p.Phe658=
NM_001142679.1:c.2028C>T	NP_001136151.1:p.Phe676=
NM_001204803.1:c.2091C>T	NP_001191732.1:p.Phe697=
XM_005268706.3:c.1995C>T	XP_005268763.1:p.Phe665=
XM_005268707.2:c.1929C>T	XP_005268764.1:p.Phe643=
XM_011538024.1:c.2091C>T	XP_011536326.1:p.Phe697=
XR_944886.1:n.1352-18491G>A
XR_944888.1:n.1352-18491G>A
XM_005268706.5:c.1995C>T	XP_005268763.1:p.Phe665=
XM_005268707.4:c.1929C>T	XP_005268764.1:p.Phe643=
XR_001749096.1:n.1353-18491G>A
XR_944886.2:n.1353-18491G>A
NM_001025356.3:c.2028C>T MANE Select	NP_001020527.2:p.Phe676=
NM_001142678.2:c.1974C>T	NP_001136150.1:p.Phe658=
NM_001142679.2:c.2028C>T	NP_001136151.1:p.Phe676=
NM_001204803.2:c.2091C>T	NP_001191732.1:p.Phe697=