Canonical Allele Identifier: CA1957393885

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218140_22218142delinsCTT , CM000673.2:g.22218140_22218142delinsCTT	GRCh38
NC_000011.9:g.22239686_22239688delinsCTT , CM000673.1:g.22239686_22239688delinsCTT	GRCh37
NC_000011.8:g.22196262_22196264delinsCTT	NCBI36
NG_015844.1:g.29965_29967delinsCTT , LRG_868:g.29965_29967delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-106_3313-104delinsCTT
ENST00000682266.1:c.-270-2957_-270-2955delinsCTT	ENSP00000507766.1:n.-270-2957_-270-2955delinsCTT
ENST00000682341.1:c.139-2957_139-2955delinsCTT	ENSP00000508251.1:n.139-2957_139-2955delinsCTT
ENST00000682530.1:c.136-603_136-601delinsCTT	ENSP00000506805.1:n.136-603_136-601delinsCTT
ENST00000682684.1:n.560-2957_560-2955delinsCTT
ENST00000683197.1:c.139-2957_139-2955delinsCTT	ENSP00000507641.1:n.139-2957_139-2955delinsCTT
ENST00000683411.1:c.-270-2957_-270-2955delinsCTT	ENSP00000508397.1:n.-270-2957_-270-2955delinsCTT
ENST00000683437.1:c.-270-2957_-270-2955delinsCTT	ENSP00000508408.1:n.-270-2957_-270-2955delinsCTT
ENST00000683834.1:n.381-2957_381-2955delinsCTT
ENST00000683897.1:n.425-2957_425-2955delinsCTT
ENST00000684365.1:n.550-2957_550-2955delinsCTT
ENST00000684663.1:c.136-2957_136-2955delinsCTT	ENSP00000508009.1:n.136-2957_136-2955delinsCTT
ENST00000324559.9:c.139-106_139-104delinsCTT MANE Select	ENSP00000315371.9:n.139-106_139-104delinsCTT
ENST00000648804.1:n.670-446_670-444delinsCTT
ENST00000324559.8:c.139-106_139-104delinsCTT	ENSP00000315371.8:n.139-106_139-104delinsCTT
NM_001142649.1:c.136-106_136-104delinsCTT	NP_001136121.1:n.136-106_136-104delinsCTT
NM_213599.2:c.139-106_139-104delinsCTT , LRG_868t1:c.139-106_139-104delinsCTT	NP_998764.1:n.139-106_139-104delinsCTT
XM_005252820.2:c.139-2957_139-2955delinsCTT	XP_005252877.2:n.139-2957_139-2955delinsCTT
XM_005252821.2:c.136-2957_136-2955delinsCTT	XP_005252878.2:n.136-2957_136-2955delinsCTT
XM_005252822.3:c.61-106_61-104delinsCTT	XP_005252879.1:n.61-106_61-104delinsCTT
XM_005252823.3:c.58-106_58-104delinsCTT	XP_005252880.1:n.58-106_58-104delinsCTT
XM_011519949.1:c.88-2957_88-2955delinsCTT	XP_011518251.1:n.88-2957_88-2955delinsCTT
XM_005252820.3:c.139-2957_139-2955delinsCTT	XP_005252877.2:n.139-2957_139-2955delinsCTT
XM_005252821.3:c.136-2957_136-2955delinsCTT	XP_005252878.2:n.136-2957_136-2955delinsCTT
XM_005252822.4:c.61-106_61-104delinsCTT	XP_005252879.1:n.61-106_61-104delinsCTT
XM_011519949.2:c.88-2957_88-2955delinsCTT	XP_011518251.1:n.88-2957_88-2955delinsCTT
NM_001142649.2:c.136-106_136-104delinsCTT	NP_001136121.1:n.136-106_136-104delinsCTT
NM_213599.3:c.139-106_139-104delinsCTT MANE Select	NP_998764.1:n.139-106_139-104delinsCTT