Canonical Allele Identifier: CA1957393811

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218043T= , CM000673.2:g.22218043T=	GRCh38
NC_000011.9:g.22239589T= , CM000673.1:g.22239589T=	GRCh37
NC_000011.8:g.22196165T=	NCBI36
NG_015844.1:g.29868T= , LRG_868:g.29868T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-203T=
ENST00000682266.1:c.-270-3054T=	ENSP00000507766.1:n.-270-3054T=
ENST00000682341.1:c.139-3054T=	ENSP00000508251.1:n.139-3054T=
ENST00000682530.1:c.136-700T=	ENSP00000506805.1:n.136-700T=
ENST00000682684.1:n.560-3054T=
ENST00000683197.1:c.139-3054T=	ENSP00000507641.1:n.139-3054T=
ENST00000683411.1:c.-270-3054T=	ENSP00000508397.1:n.-270-3054T=
ENST00000683437.1:c.-270-3054T=	ENSP00000508408.1:n.-270-3054T=
ENST00000683834.1:n.381-3054T=
ENST00000683897.1:n.425-3054T=
ENST00000684365.1:n.550-3054T=
ENST00000684663.1:c.136-3054T=	ENSP00000508009.1:n.136-3054T=
ENST00000324559.9:c.139-203T= MANE Select	ENSP00000315371.9:n.139-203T=
ENST00000648804.1:n.670-543T=
ENST00000324559.8:c.139-203T=	ENSP00000315371.8:n.139-203T=
NM_001142649.1:c.136-203T=	NP_001136121.1:n.136-203T=
NM_213599.2:c.139-203T= , LRG_868t1:c.139-203T=	NP_998764.1:n.139-203T=
XM_005252820.2:c.139-3054T=	XP_005252877.2:n.139-3054T=
XM_005252821.2:c.136-3054T=	XP_005252878.2:n.136-3054T=
XM_005252822.3:c.61-203T=	XP_005252879.1:n.61-203T=
XM_005252823.3:c.58-203T=	XP_005252880.1:n.58-203T=
XM_011519949.1:c.88-3054T=	XP_011518251.1:n.88-3054T=
XM_005252820.3:c.139-3054T=	XP_005252877.2:n.139-3054T=
XM_005252821.3:c.136-3054T=	XP_005252878.2:n.136-3054T=
XM_005252822.4:c.61-203T=	XP_005252879.1:n.61-203T=
XM_011519949.2:c.88-3054T=	XP_011518251.1:n.88-3054T=
NM_001142649.2:c.136-203T=	NP_001136121.1:n.136-203T=
NM_213599.3:c.139-203T= MANE Select	NP_998764.1:n.139-203T=