Canonical Allele Identifier: CA1957419832

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262189_22262212delinsAGTTTGTAAATTTTTACTCATCCT , CM000673.2:g.22262189_22262212delinsAGTTTGTAAATTTTTACTCATCCT	GRCh38
NC_000011.9:g.22283735_22283758delinsAGTTTGTAAATTTTTACTCATCCT , CM000673.1:g.22283735_22283758delinsAGTTTGTAAATTTTTACTCATCCT	GRCh37
NC_000011.8:g.22240311_22240334delinsAGTTTGTAAATTTTTACTCATCCT	NCBI36
NG_015844.1:g.74014_74037delinsAGTTTGTAAATTTTTACTCATCCT , LRG_868:g.74014_74037delinsAGTTTGTAAATTTTTACTCATCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1241_1264delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000507766.1:p.Gln414=
ENST00000682341.1:c.1649_1672delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000508251.1:p.Gln550=
ENST00000683197.1:c.1649_1672delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000507641.1:p.Gln550=
ENST00000683411.1:c.1241_1264delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000508397.1:p.Gln414=
ENST00000683437.1:c.1241_1264delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000508408.1:p.Gln414=
ENST00000683613.1:n.2685_2708delinsAGTTTGTAAATTTTTACTCATCCT
ENST00000684663.1:c.1646_1669delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000508009.1:p.Gln549=
ENST00000324559.9:c.1691_1714delinsAGTTTGTAAATTTTTACTCATCCT MANE Select	ENSP00000315371.9:p.Gln564=
ENST00000648804.1:n.2026_2049delinsAGTTTGTAAATTTTTACTCATCCT
ENST00000324559.8:c.1691_1714delinsAGTTTGTAAATTTTTACTCATCCT	ENSP00000315371.8:p.Gln564=
NM_001142649.1:c.1688_1711delinsAGTTTGTAAATTTTTACTCATCCT	NP_001136121.1:p.Gln563=
NM_213599.2:c.1691_1714delinsAGTTTGTAAATTTTTACTCATCCT , LRG_868t1:c.1691_1714delinsAGTTTGTAAATTTTTACTCATCCT	NP_998764.1:p.Gln564=
XM_005252820.2:c.1649_1672delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252877.2:p.Gln550=
XM_005252821.2:c.1646_1669delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252878.2:p.Gln549=
XM_005252822.3:c.1613_1636delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252879.1:p.Gln538=
XM_005252823.3:c.1610_1633delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252880.1:p.Gln537=
XM_011519949.1:c.1598_1621delinsAGTTTGTAAATTTTTACTCATCCT	XP_011518251.1:p.Gln533=
XM_005252820.3:c.1649_1672delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252877.2:p.Gln550=
XM_005252821.3:c.1646_1669delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252878.2:p.Gln549=
XM_005252822.4:c.1613_1636delinsAGTTTGTAAATTTTTACTCATCCT	XP_005252879.1:p.Gln538=
XM_011519949.2:c.1598_1621delinsAGTTTGTAAATTTTTACTCATCCT	XP_011518251.1:p.Gln533=
NM_001142649.2:c.1688_1711delinsAGTTTGTAAATTTTTACTCATCCT	NP_001136121.1:p.Gln563=
NM_213599.3:c.1691_1714delinsAGTTTGTAAATTTTTACTCATCCT MANE Select	NP_998764.1:p.Gln564=