Canonical Allele Identifier: CA2033289913

Gene: ANO6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45403435C= , CM000674.2:g.45403435C=	GRCh38
NC_000012.11:g.45797218C= , CM000674.1:g.45797218C=	GRCh37
NC_000012.10:g.44083485C=	NCBI36
NG_028220.1:g.192449C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320560.13:c.1783-4C= MANE Select	ENSP00000320087.8:n.1783-4C=
ENST00000679426.1:c.1750-4C=	ENSP00000506600.1:n.1750-4C=
ENST00000679761.1:c.1783-4C=	ENSP00000505361.1:n.1783-4C=
ENST00000680201.1:c.1783-4C=	ENSP00000506222.1:n.1783-4C=
ENST00000680371.1:c.1783-4C=	ENSP00000506392.1:n.1783-4C=
ENST00000680498.1:c.1366-4C=	ENSP00000506613.1:n.1366-4C=
ENST00000681156.1:c.1783-4C=	ENSP00000506069.1:n.1783-4C=
ENST00000681817.1:c.1366-4C=	ENSP00000506683.1:n.1366-4C=
ENST00000320560.12:c.1783-4C=	ENSP00000320087.8:n.1783-4C=
ENST00000423947.7:c.1846-4C=	ENSP00000409126.3:n.1846-4C=
ENST00000425752.6:c.1783-4C=	ENSP00000391417.2:n.1783-4C=
ENST00000426898.2:n.2199-4C=
ENST00000441606.2:c.1729-4C=	ENSP00000413137.2:n.1729-4C=
NM_001025356.2:c.1783-4C=	NP_001020527.2:n.1783-4C=
NM_001142678.1:c.1729-4C=	NP_001136150.1:n.1729-4C=
NM_001142679.1:c.1783-4C=	NP_001136151.1:n.1783-4C=
NM_001204803.1:c.1846-4C=	NP_001191732.1:n.1846-4C=
XM_005268706.3:c.1750-4C=	XP_005268763.1:n.1750-4C=
XM_005268707.2:c.1684-4C=	XP_005268764.1:n.1684-4C=
XM_011538024.1:c.1846-4C=	XP_011536326.1:n.1846-4C=
XR_944886.1:n.1352-5211G=
XR_944888.1:n.1352-5211G=
XM_005268706.5:c.1750-4C=	XP_005268763.1:n.1750-4C=
XM_005268707.4:c.1684-4C=	XP_005268764.1:n.1684-4C=
XR_001749096.1:n.1353-5211G=
XR_944886.2:n.1353-5211G=
NM_001025356.3:c.1783-4C= MANE Select	NP_001020527.2:n.1783-4C=
NM_001142678.2:c.1729-4C=	NP_001136150.1:n.1729-4C=
NM_001142679.2:c.1783-4C=	NP_001136151.1:n.1783-4C=
NM_001204803.2:c.1846-4C=	NP_001191732.1:n.1846-4C=