Canonical Allele Identifier: CA1957403529

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22273205_22273208delinsTATC , CM000673.2:g.22273205_22273208delinsTATC	GRCh38
NC_000011.9:g.22294751_22294754delinsTATC , CM000673.1:g.22294751_22294754delinsTATC	GRCh37
NC_000011.8:g.22251327_22251330delinsTATC	NCBI36
NG_015844.1:g.85030_85033delinsTATC , LRG_868:g.85030_85033delinsTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.252+216_252+219delinsTATC
ENST00000682266.1:c.1785+216_1785+219delinsTATC	ENSP00000507766.1:n.1785+216_1785+219delinsTATC
ENST00000682341.1:c.2193+216_2193+219delinsTATC	ENSP00000508251.1:n.2193+216_2193+219delinsTATC
ENST00000683197.1:c.2193+216_2193+219delinsTATC	ENSP00000507641.1:n.2193+216_2193+219delinsTATC
ENST00000683411.1:c.1785+216_1785+219delinsTATC	ENSP00000508397.1:n.1785+216_1785+219delinsTATC
ENST00000683437.1:c.1785+216_1785+219delinsTATC	ENSP00000508408.1:n.1785+216_1785+219delinsTATC
ENST00000683613.1:n.3229+216_3229+219delinsTATC
ENST00000684663.1:c.2190+216_2190+219delinsTATC	ENSP00000508009.1:n.2190+216_2190+219delinsTATC
ENST00000324559.9:c.2235+216_2235+219delinsTATC MANE Select	ENSP00000315371.9:n.2235+216_2235+219delinsTATC
ENST00000648804.1:n.2570+216_2570+219delinsTATC
ENST00000324559.8:c.2235+216_2235+219delinsTATC	ENSP00000315371.8:n.2235+216_2235+219delinsTATC
ENST00000532043.1:n.252+216_252+219delinsTATC
NM_001142649.1:c.2232+216_2232+219delinsTATC	NP_001136121.1:n.2232+216_2232+219delinsTATC
NM_213599.2:c.2235+216_2235+219delinsTATC , LRG_868t1:c.2235+216_2235+219delinsTATC	NP_998764.1:n.2235+216_2235+219delinsTATC
XM_005252820.2:c.2193+216_2193+219delinsTATC	XP_005252877.2:n.2193+216_2193+219delinsTATC
XM_005252821.2:c.2190+216_2190+219delinsTATC	XP_005252878.2:n.2190+216_2190+219delinsTATC
XM_005252822.3:c.2157+216_2157+219delinsTATC	XP_005252879.1:n.2157+216_2157+219delinsTATC
XM_005252823.3:c.2154+216_2154+219delinsTATC	XP_005252880.1:n.2154+216_2154+219delinsTATC
XM_011519949.1:c.2142+216_2142+219delinsTATC	XP_011518251.1:n.2142+216_2142+219delinsTATC
XM_005252820.3:c.2193+216_2193+219delinsTATC	XP_005252877.2:n.2193+216_2193+219delinsTATC
XM_005252821.3:c.2190+216_2190+219delinsTATC	XP_005252878.2:n.2190+216_2190+219delinsTATC
XM_005252822.4:c.2157+216_2157+219delinsTATC	XP_005252879.1:n.2157+216_2157+219delinsTATC
XM_011519949.2:c.2142+216_2142+219delinsTATC	XP_011518251.1:n.2142+216_2142+219delinsTATC
NM_001142649.2:c.2232+216_2232+219delinsTATC	NP_001136121.1:n.2232+216_2232+219delinsTATC
NM_213599.3:c.2235+216_2235+219delinsTATC MANE Select	NP_998764.1:n.2235+216_2235+219delinsTATC