Canonical Allele Identifier: CA1957403012

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272922_22272929delinsAAGCTCAT , CM000673.2:g.22272922_22272929delinsAAGCTCAT	GRCh38
NC_000011.9:g.22294468_22294475delinsAAGCTCAT , CM000673.1:g.22294468_22294475delinsAAGCTCAT	GRCh37
NC_000011.8:g.22251044_22251051delinsAAGCTCAT	NCBI36
NG_015844.1:g.84747_84754delinsAAGCTCAT , LRG_868:g.84747_84754delinsAAGCTCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.185_192delinsAAGCTCAT
ENST00000682266.1:c.1718_1725delinsAAGCTCAT	ENSP00000507766.1:p.Lys573=
ENST00000682341.1:c.2126_2133delinsAAGCTCAT	ENSP00000508251.1:p.Lys709=
ENST00000683197.1:c.2126_2133delinsAAGCTCAT	ENSP00000507641.1:p.Lys709=
ENST00000683411.1:c.1718_1725delinsAAGCTCAT	ENSP00000508397.1:p.Lys573=
ENST00000683437.1:c.1718_1725delinsAAGCTCAT	ENSP00000508408.1:p.Lys573=
ENST00000683613.1:n.3162_3169delinsAAGCTCAT
ENST00000684663.1:c.2123_2130delinsAAGCTCAT	ENSP00000508009.1:p.Lys708=
ENST00000324559.9:c.2168_2175delinsAAGCTCAT MANE Select	ENSP00000315371.9:p.Lys723=
ENST00000648804.1:n.2503_2510delinsAAGCTCAT
ENST00000324559.8:c.2168_2175delinsAAGCTCAT	ENSP00000315371.8:p.Lys723=
ENST00000532043.1:n.185_192delinsAAGCTCAT
NM_001142649.1:c.2165_2172delinsAAGCTCAT	NP_001136121.1:p.Lys722=
NM_213599.2:c.2168_2175delinsAAGCTCAT , LRG_868t1:c.2168_2175delinsAAGCTCAT	NP_998764.1:p.Lys723=
XM_005252820.2:c.2126_2133delinsAAGCTCAT	XP_005252877.2:p.Lys709=
XM_005252821.2:c.2123_2130delinsAAGCTCAT	XP_005252878.2:p.Lys708=
XM_005252822.3:c.2090_2097delinsAAGCTCAT	XP_005252879.1:p.Lys697=
XM_005252823.3:c.2087_2094delinsAAGCTCAT	XP_005252880.1:p.Lys696=
XM_011519949.1:c.2075_2082delinsAAGCTCAT	XP_011518251.1:p.Lys692=
XM_005252820.3:c.2126_2133delinsAAGCTCAT	XP_005252877.2:p.Lys709=
XM_005252821.3:c.2123_2130delinsAAGCTCAT	XP_005252878.2:p.Lys708=
XM_005252822.4:c.2090_2097delinsAAGCTCAT	XP_005252879.1:p.Lys697=
XM_011519949.2:c.2075_2082delinsAAGCTCAT	XP_011518251.1:p.Lys692=
NM_001142649.2:c.2165_2172delinsAAGCTCAT	NP_001136121.1:p.Lys722=
NM_213599.3:c.2168_2175delinsAAGCTCAT MANE Select	NP_998764.1:p.Lys723=