Canonical Allele Identifier: CA1957393867

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218123A= , CM000673.2:g.22218123A=	GRCh38
NC_000011.9:g.22239669A= , CM000673.1:g.22239669A=	GRCh37
NC_000011.8:g.22196245A=	NCBI36
NG_015844.1:g.29948A= , LRG_868:g.29948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-123A=
ENST00000682266.1:c.-270-2974A=	ENSP00000507766.1:n.-270-2974A=
ENST00000682341.1:c.139-2974A=	ENSP00000508251.1:n.139-2974A=
ENST00000682530.1:c.136-620A=	ENSP00000506805.1:n.136-620A=
ENST00000682684.1:n.560-2974A=
ENST00000683197.1:c.139-2974A=	ENSP00000507641.1:n.139-2974A=
ENST00000683411.1:c.-270-2974A=	ENSP00000508397.1:n.-270-2974A=
ENST00000683437.1:c.-270-2974A=	ENSP00000508408.1:n.-270-2974A=
ENST00000683834.1:n.381-2974A=
ENST00000683897.1:n.425-2974A=
ENST00000684365.1:n.550-2974A=
ENST00000684663.1:c.136-2974A=	ENSP00000508009.1:n.136-2974A=
ENST00000324559.9:c.139-123A= MANE Select	ENSP00000315371.9:n.139-123A=
ENST00000648804.1:n.670-463A=
ENST00000324559.8:c.139-123A=	ENSP00000315371.8:n.139-123A=
NM_001142649.1:c.136-123A=	NP_001136121.1:n.136-123A=
NM_213599.2:c.139-123A= , LRG_868t1:c.139-123A=	NP_998764.1:n.139-123A=
XM_005252820.2:c.139-2974A=	XP_005252877.2:n.139-2974A=
XM_005252821.2:c.136-2974A=	XP_005252878.2:n.136-2974A=
XM_005252822.3:c.61-123A=	XP_005252879.1:n.61-123A=
XM_005252823.3:c.58-123A=	XP_005252880.1:n.58-123A=
XM_011519949.1:c.88-2974A=	XP_011518251.1:n.88-2974A=
XM_005252820.3:c.139-2974A=	XP_005252877.2:n.139-2974A=
XM_005252821.3:c.136-2974A=	XP_005252878.2:n.136-2974A=
XM_005252822.4:c.61-123A=	XP_005252879.1:n.61-123A=
XM_011519949.2:c.88-2974A=	XP_011518251.1:n.88-2974A=
NM_001142649.2:c.136-123A=	NP_001136121.1:n.136-123A=
NM_213599.3:c.139-123A= MANE Select	NP_998764.1:n.139-123A=