Canonical Allele Identifier: CA379921609

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255485C>T , CM000673.2:g.22255485C>T	GRCh38
NC_000011.9:g.22277031C>T , CM000673.1:g.22277031C>T	GRCh37
NC_000011.8:g.22233607C>T	NCBI36
NG_015844.1:g.67310C>T , LRG_868:g.67310C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1295C>T MANE Select	NP_998764.1:p.Ala432Val
ENST00000324559.9:c.1295C>T MANE Select	ENSP00000315371.9:p.Ala432Val
NM_001142649.1:c.1292C>T	NP_001136121.1:p.Ala431Val
NM_001142649.2:c.1292C>T	NP_001136121.1:p.Ala431Val
NM_213599.2:c.1295C>T , LRG_868t1:c.1295C>T	NP_998764.1:p.Ala432Val
ENST00000324559.8:c.1295C>T	ENSP00000315371.8:p.Ala432Val
ENST00000648804.1:n.1630C>T
ENST00000682089.1:n.615C>T
ENST00000682266.1:c.845C>T	ENSP00000507766.1:p.Ala282Val
ENST00000682341.1:c.1253C>T	ENSP00000508251.1:p.Ala418Val
ENST00000682530.1:c.*1227C>T	ENSP00000506805.1:n.*1227C>T
ENST00000683197.1:c.1253C>T	ENSP00000507641.1:p.Ala418Val
ENST00000683411.1:c.845C>T	ENSP00000508397.1:p.Ala282Val
ENST00000683437.1:c.845C>T	ENSP00000508408.1:p.Ala282Val
ENST00000683613.1:n.2289C>T
ENST00000683834.1:n.1495C>T
ENST00000684663.1:c.1250C>T	ENSP00000508009.1:p.Ala417Val
XM_005252820.2:c.1253C>T	XP_005252877.2:p.Ala418Val
XM_005252820.3:c.1253C>T	XP_005252877.2:p.Ala418Val
XM_005252821.2:c.1250C>T	XP_005252878.2:p.Ala417Val
XM_005252821.3:c.1250C>T	XP_005252878.2:p.Ala417Val
XM_005252822.3:c.1217C>T	XP_005252879.1:p.Ala406Val
XM_005252822.4:c.1217C>T	XP_005252879.1:p.Ala406Val
XM_005252823.3:c.1214C>T	XP_005252880.1:p.Ala405Val
XM_011519949.1:c.1202C>T	XP_011518251.1:p.Ala401Val
XM_011519949.2:c.1202C>T	XP_011518251.1:p.Ala401Val