Canonical Allele Identifier: CA6525195

Gene: ANO6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45367805T>G , CM000674.2:g.45367805T>G	GRCh38
NC_000012.11:g.45761588T>G , CM000674.1:g.45761588T>G	GRCh37
NC_000012.10:g.44047855T>G	NCBI36
NG_028220.1:g.156819T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320560.13:c.1104+12T>G MANE Select	ENSP00000320087.8:n.1104+12T>G
ENST00000679426.1:c.1071+12T>G	ENSP00000506600.1:n.1071+12T>G
ENST00000679761.1:c.1104+12T>G	ENSP00000505361.1:n.1104+12T>G
ENST00000680201.1:c.1104+12T>G	ENSP00000506222.1:n.1104+12T>G
ENST00000680371.1:c.1104+12T>G	ENSP00000506392.1:n.1104+12T>G
ENST00000680498.1:c.687+12T>G	ENSP00000506613.1:n.687+12T>G
ENST00000681156.1:c.1104+12T>G	ENSP00000506069.1:n.1104+12T>G
ENST00000681817.1:c.687+12T>G	ENSP00000506683.1:n.687+12T>G
ENST00000320560.12:c.1104+12T>G	ENSP00000320087.8:n.1104+12T>G
ENST00000423947.7:c.1167+12T>G	ENSP00000409126.3:n.1167+12T>G
ENST00000425752.6:c.1104+12T>G	ENSP00000391417.2:n.1104+12T>G
ENST00000426898.2:n.1359+12T>G
ENST00000441606.2:c.1050+12T>G	ENSP00000413137.2:n.1050+12T>G
NM_001025356.2:c.1104+12T>G	NP_001020527.2:n.1104+12T>G
NM_001142678.1:c.1050+12T>G	NP_001136150.1:n.1050+12T>G
NM_001142679.1:c.1104+12T>G	NP_001136151.1:n.1104+12T>G
NM_001204803.1:c.1167+12T>G	NP_001191732.1:n.1167+12T>G
XM_005268706.3:c.1071+12T>G	XP_005268763.1:n.1071+12T>G
XM_005268707.2:c.1005+12T>G	XP_005268764.1:n.1005+12T>G
XM_011538024.1:c.1167+12T>G	XP_011536326.1:n.1167+12T>G
XM_005268706.5:c.1071+12T>G	XP_005268763.1:n.1071+12T>G
XM_005268707.4:c.1005+12T>G	XP_005268764.1:n.1005+12T>G
NM_001025356.3:c.1104+12T>G MANE Select	NP_001020527.2:n.1104+12T>G
NM_001142678.2:c.1050+12T>G	NP_001136150.1:n.1050+12T>G
NM_001142679.2:c.1104+12T>G	NP_001136151.1:n.1104+12T>G
NM_001204803.2:c.1167+12T>G	NP_001191732.1:n.1167+12T>G