Canonical Allele Identifier: CA5923458

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272870C>T , CM000673.2:g.22272870C>T	GRCh38
NC_000011.9:g.22294416C>T , CM000673.1:g.22294416C>T	GRCh37
NC_000011.8:g.22250992C>T	NCBI36
NG_015844.1:g.84695C>T , LRG_868:g.84695C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.2116C>T MANE Select	NP_998764.1:p.Arg706Ter
ENST00000324559.9:c.2116C>T MANE Select	ENSP00000315371.9:p.Arg706Ter
NM_001142649.1:c.2113C>T	NP_001136121.1:p.Arg705Ter
NM_001142649.2:c.2113C>T	NP_001136121.1:p.Arg705Ter
NM_213599.2:c.2116C>T , LRG_868t1:c.2116C>T	NP_998764.1:p.Arg706Ter
ENST00000324559.8:c.2116C>T	ENSP00000315371.8:p.Arg706Ter
ENST00000532043.1:n.133C>T
ENST00000532043.2:n.133C>T
ENST00000648804.1:n.2451C>T
ENST00000682266.1:c.1666C>T	ENSP00000507766.1:p.Arg556Ter
ENST00000682341.1:c.2074C>T	ENSP00000508251.1:p.Arg692Ter
ENST00000683197.1:c.2074C>T	ENSP00000507641.1:p.Arg692Ter
ENST00000683411.1:c.1666C>T	ENSP00000508397.1:p.Arg556Ter
ENST00000683437.1:c.1666C>T	ENSP00000508408.1:p.Arg556Ter
ENST00000683613.1:n.3110C>T
ENST00000684663.1:c.2071C>T	ENSP00000508009.1:p.Arg691Ter
XM_005252820.2:c.2074C>T	XP_005252877.2:p.Arg692Ter
XM_005252820.3:c.2074C>T	XP_005252877.2:p.Arg692Ter
XM_005252821.2:c.2071C>T	XP_005252878.2:p.Arg691Ter
XM_005252821.3:c.2071C>T	XP_005252878.2:p.Arg691Ter
XM_005252822.3:c.2038C>T	XP_005252879.1:p.Arg680Ter
XM_005252822.4:c.2038C>T	XP_005252879.1:p.Arg680Ter
XM_005252823.3:c.2035C>T	XP_005252880.1:p.Arg679Ter
XM_011519949.1:c.2023C>T	XP_011518251.1:p.Arg675Ter
XM_011519949.2:c.2023C>T	XP_011518251.1:p.Arg675Ter