Canonical Allele Identifier: CA1957416920

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255405A= , CM000673.2:g.22255405A=	GRCh38
NC_000011.9:g.22276951A= , CM000673.1:g.22276951A=	GRCh37
NC_000011.8:g.22233527A=	NCBI36
NG_015844.1:g.67230A= , LRG_868:g.67230A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.535A=
ENST00000682266.1:c.765A=	ENSP00000507766.1:p.Gln255=
ENST00000682341.1:c.1173A=	ENSP00000508251.1:p.Gln391=
ENST00000682530.1:c.*1147A=	ENSP00000506805.1:n.*1147A=
ENST00000683197.1:c.1173A=	ENSP00000507641.1:p.Gln391=
ENST00000683411.1:c.765A=	ENSP00000508397.1:p.Gln255=
ENST00000683437.1:c.765A=	ENSP00000508408.1:p.Gln255=
ENST00000683613.1:n.2209A=
ENST00000683834.1:n.1415A=
ENST00000684663.1:c.1170A=	ENSP00000508009.1:p.Gln390=
ENST00000324559.9:c.1215A= MANE Select	ENSP00000315371.9:p.Gln405=
ENST00000648804.1:n.1550A=
ENST00000324559.8:c.1215A=	ENSP00000315371.8:p.Gln405=
NM_001142649.1:c.1212A=	NP_001136121.1:p.Gln404=
NM_213599.2:c.1215A= , LRG_868t1:c.1215A=	NP_998764.1:p.Gln405=
XM_005252820.2:c.1173A=	XP_005252877.2:p.Gln391=
XM_005252821.2:c.1170A=	XP_005252878.2:p.Gln390=
XM_005252822.3:c.1137A=	XP_005252879.1:p.Gln379=
XM_005252823.3:c.1134A=	XP_005252880.1:p.Gln378=
XM_011519949.1:c.1122A=	XP_011518251.1:p.Gln374=
XM_005252820.3:c.1173A=	XP_005252877.2:p.Gln391=
XM_005252821.3:c.1170A=	XP_005252878.2:p.Gln390=
XM_005252822.4:c.1137A=	XP_005252879.1:p.Gln379=
XM_011519949.2:c.1122A=	XP_011518251.1:p.Gln374=
NM_001142649.2:c.1212A=	NP_001136121.1:p.Gln404=
NM_213599.3:c.1215A= MANE Select	NP_998764.1:p.Gln405=