Canonical Allele Identifier: CA6400994

Gene: ANO2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.5832446A>T , CM000674.2:g.5832446A>T	GRCh38
NC_000012.11:g.5941612A>T , CM000674.1:g.5941612A>T	GRCh37
NC_000012.10:g.5811873A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001364791.2:c.785+6T>A MANE Select	NP_001351720.1:n.785+6T>A
ENST00000682330.1:c.785+6T>A MANE Select	ENSP00000507275.1:n.785+6T>A
NM_001278596.1:c.788+6T>A	NP_001265525.1:n.788+6T>A
NM_001278596.2:c.788+6T>A	NP_001265525.1:n.788+6T>A
NM_001278596.3:c.788+6T>A	NP_001265525.1:n.788+6T>A
NM_001278597.1:c.776+6T>A	NP_001265526.1:n.776+6T>A
NM_001278597.2:c.776+6T>A	NP_001265526.1:n.776+6T>A
NM_001278597.3:c.776+6T>A	NP_001265526.1:n.776+6T>A
NM_001364791.1:c.785+6T>A	NP_001351720.1:n.785+6T>A
ENST00000327087.12:c.776+6T>A	ENSP00000314048.9:n.776+6T>A
ENST00000356134.9:c.776+6T>A	ENSP00000348453.5:n.776+6T>A
ENST00000544988.1:n.453+6T>A
ENST00000546188.5:c.788+6T>A	ENSP00000440981.2:n.788+6T>A
ENST00000650848.1:c.788+6T>A	ENSP00000498903.1:n.788+6T>A
XM_006718988.2:c.785+6T>A	XP_006719051.1:n.785+6T>A
XM_011520975.1:c.773+6T>A	XP_011519277.1:n.773+6T>A
XM_011520975.2:c.773+6T>A	XP_011519277.1:n.773+6T>A
XM_011520976.1:c.668+6T>A	XP_011519278.1:n.668+6T>A
XM_011520977.1:c.254+6T>A	XP_011519279.1:n.254+6T>A
XM_011520978.1:c.152+6T>A	XP_011519280.1:n.152+6T>A
XM_011520978.3:c.152+6T>A	XP_011519280.1:n.152+6T>A
XM_017019672.2:c.785+6T>A	XP_016875161.1:n.785+6T>A
XM_024449073.1:c.668+6T>A	XP_024304841.1:n.668+6T>A
XR_002957363.1:n.4358+6T>A
XR_931519.1:n.1117+6T>A
XR_931519.2:n.4358+6T>A