Canonical Allele Identifier: CA1957393819

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218072_22218076delinsCTTCT , CM000673.2:g.22218072_22218076delinsCTTCT	GRCh38
NC_000011.9:g.22239618_22239622delinsCTTCT , CM000673.1:g.22239618_22239622delinsCTTCT	GRCh37
NC_000011.8:g.22196194_22196198delinsCTTCT	NCBI36
NG_015844.1:g.29897_29901delinsCTTCT , LRG_868:g.29897_29901delinsCTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682084.1:n.3313-174_3313-170delinsCTTCT
ENST00000682266.1:c.-270-3025_-270-3021delinsCTTCT	ENSP00000507766.1:n.-270-3025_-270-3021delinsCTTCT
ENST00000682341.1:c.139-3025_139-3021delinsCTTCT	ENSP00000508251.1:n.139-3025_139-3021delinsCTTCT
ENST00000682530.1:c.136-671_136-667delinsCTTCT	ENSP00000506805.1:n.136-671_136-667delinsCTTCT
ENST00000682684.1:n.560-3025_560-3021delinsCTTCT
ENST00000683197.1:c.139-3025_139-3021delinsCTTCT	ENSP00000507641.1:n.139-3025_139-3021delinsCTTCT
ENST00000683411.1:c.-270-3025_-270-3021delinsCTTCT	ENSP00000508397.1:n.-270-3025_-270-3021delinsCTTCT
ENST00000683437.1:c.-270-3025_-270-3021delinsCTTCT	ENSP00000508408.1:n.-270-3025_-270-3021delinsCTTCT
ENST00000683834.1:n.381-3025_381-3021delinsCTTCT
ENST00000683897.1:n.425-3025_425-3021delinsCTTCT
ENST00000684365.1:n.550-3025_550-3021delinsCTTCT
ENST00000684663.1:c.136-3025_136-3021delinsCTTCT	ENSP00000508009.1:n.136-3025_136-3021delinsCTTCT
ENST00000324559.9:c.139-174_139-170delinsCTTCT MANE Select	ENSP00000315371.9:n.139-174_139-170delinsCTTCT
ENST00000648804.1:n.670-514_670-510delinsCTTCT
ENST00000324559.8:c.139-174_139-170delinsCTTCT	ENSP00000315371.8:n.139-174_139-170delinsCTTCT
NM_001142649.1:c.136-174_136-170delinsCTTCT	NP_001136121.1:n.136-174_136-170delinsCTTCT
NM_213599.2:c.139-174_139-170delinsCTTCT , LRG_868t1:c.139-174_139-170delinsCTTCT	NP_998764.1:n.139-174_139-170delinsCTTCT
XM_005252820.2:c.139-3025_139-3021delinsCTTCT	XP_005252877.2:n.139-3025_139-3021delinsCTTCT
XM_005252821.2:c.136-3025_136-3021delinsCTTCT	XP_005252878.2:n.136-3025_136-3021delinsCTTCT
XM_005252822.3:c.61-174_61-170delinsCTTCT	XP_005252879.1:n.61-174_61-170delinsCTTCT
XM_005252823.3:c.58-174_58-170delinsCTTCT	XP_005252880.1:n.58-174_58-170delinsCTTCT
XM_011519949.1:c.88-3025_88-3021delinsCTTCT	XP_011518251.1:n.88-3025_88-3021delinsCTTCT
XM_005252820.3:c.139-3025_139-3021delinsCTTCT	XP_005252877.2:n.139-3025_139-3021delinsCTTCT
XM_005252821.3:c.136-3025_136-3021delinsCTTCT	XP_005252878.2:n.136-3025_136-3021delinsCTTCT
XM_005252822.4:c.61-174_61-170delinsCTTCT	XP_005252879.1:n.61-174_61-170delinsCTTCT
XM_011519949.2:c.88-3025_88-3021delinsCTTCT	XP_011518251.1:n.88-3025_88-3021delinsCTTCT
NM_001142649.2:c.136-174_136-170delinsCTTCT	NP_001136121.1:n.136-174_136-170delinsCTTCT
NM_213599.3:c.139-174_139-170delinsCTTCT MANE Select	NP_998764.1:n.139-174_139-170delinsCTTCT