Canonical Allele Identifier: CA10604844

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22274570C>A , CM000673.2:g.22274570C>A	GRCh38
NC_000011.9:g.22296116C>A , CM000673.1:g.22296116C>A	GRCh37
NC_000011.8:g.22252692C>A	NCBI36
NG_015844.1:g.86395C>A , LRG_868:g.86395C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.2237C>A MANE Select	NP_998764.1:p.Ala746Asp
ENST00000324559.9:c.2237C>A MANE Select	ENSP00000315371.9:p.Ala746Asp
NM_001142649.1:c.2234C>A	NP_001136121.1:p.Ala745Asp
NM_001142649.2:c.2234C>A	NP_001136121.1:p.Ala745Asp
NM_213599.2:c.2237C>A , LRG_868t1:c.2237C>A	NP_998764.1:p.Ala746Asp
ENST00000324559.8:c.2237C>A	ENSP00000315371.8:p.Ala746Asp
ENST00000532043.1:n.254C>A
ENST00000532043.2:n.254C>A
ENST00000648804.1:n.2572C>A
ENST00000682266.1:c.1787C>A	ENSP00000507766.1:p.Ala596Asp
ENST00000682341.1:c.2195C>A	ENSP00000508251.1:p.Ala732Asp
ENST00000683197.1:c.2195C>A	ENSP00000507641.1:p.Ala732Asp
ENST00000683411.1:c.1787C>A	ENSP00000508397.1:p.Ala596Asp
ENST00000683437.1:c.1787C>A	ENSP00000508408.1:p.Ala596Asp
ENST00000683613.1:n.3231C>A
ENST00000684663.1:c.2192C>A	ENSP00000508009.1:p.Ala731Asp
XM_005252820.2:c.2195C>A	XP_005252877.2:p.Ala732Asp
XM_005252820.3:c.2195C>A	XP_005252877.2:p.Ala732Asp
XM_005252821.2:c.2192C>A	XP_005252878.2:p.Ala731Asp
XM_005252821.3:c.2192C>A	XP_005252878.2:p.Ala731Asp
XM_005252822.3:c.2159C>A	XP_005252879.1:p.Ala720Asp
XM_005252822.4:c.2159C>A	XP_005252879.1:p.Ala720Asp
XM_005252823.3:c.2156C>A	XP_005252880.1:p.Ala719Asp
XM_011519949.1:c.2144C>A	XP_011518251.1:p.Ala715Asp
XM_011519949.2:c.2144C>A	XP_011518251.1:p.Ala715Asp