Canonical Allele Identifier: CA1957403536

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22273211_22273213delinsGAC , CM000673.2:g.22273211_22273213delinsGAC	GRCh38
NC_000011.9:g.22294757_22294759delinsGAC , CM000673.1:g.22294757_22294759delinsGAC	GRCh37
NC_000011.8:g.22251333_22251335delinsGAC	NCBI36
NG_015844.1:g.85036_85038delinsGAC , LRG_868:g.85036_85038delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.252+222_252+224delinsGAC
ENST00000682266.1:c.1785+222_1785+224delinsGAC	ENSP00000507766.1:n.1785+222_1785+224delinsGAC
ENST00000682341.1:c.2193+222_2193+224delinsGAC	ENSP00000508251.1:n.2193+222_2193+224delinsGAC
ENST00000683197.1:c.2193+222_2193+224delinsGAC	ENSP00000507641.1:n.2193+222_2193+224delinsGAC
ENST00000683411.1:c.1785+222_1785+224delinsGAC	ENSP00000508397.1:n.1785+222_1785+224delinsGAC
ENST00000683437.1:c.1785+222_1785+224delinsGAC	ENSP00000508408.1:n.1785+222_1785+224delinsGAC
ENST00000683613.1:n.3229+222_3229+224delinsGAC
ENST00000684663.1:c.2190+222_2190+224delinsGAC	ENSP00000508009.1:n.2190+222_2190+224delinsGAC
ENST00000324559.9:c.2235+222_2235+224delinsGAC MANE Select	ENSP00000315371.9:n.2235+222_2235+224delinsGAC
ENST00000648804.1:n.2570+222_2570+224delinsGAC
ENST00000324559.8:c.2235+222_2235+224delinsGAC	ENSP00000315371.8:n.2235+222_2235+224delinsGAC
ENST00000532043.1:n.252+222_252+224delinsGAC
NM_001142649.1:c.2232+222_2232+224delinsGAC	NP_001136121.1:n.2232+222_2232+224delinsGAC
NM_213599.2:c.2235+222_2235+224delinsGAC , LRG_868t1:c.2235+222_2235+224delinsGAC	NP_998764.1:n.2235+222_2235+224delinsGAC
XM_005252820.2:c.2193+222_2193+224delinsGAC	XP_005252877.2:n.2193+222_2193+224delinsGAC
XM_005252821.2:c.2190+222_2190+224delinsGAC	XP_005252878.2:n.2190+222_2190+224delinsGAC
XM_005252822.3:c.2157+222_2157+224delinsGAC	XP_005252879.1:n.2157+222_2157+224delinsGAC
XM_005252823.3:c.2154+222_2154+224delinsGAC	XP_005252880.1:n.2154+222_2154+224delinsGAC
XM_011519949.1:c.2142+222_2142+224delinsGAC	XP_011518251.1:n.2142+222_2142+224delinsGAC
XM_005252820.3:c.2193+222_2193+224delinsGAC	XP_005252877.2:n.2193+222_2193+224delinsGAC
XM_005252821.3:c.2190+222_2190+224delinsGAC	XP_005252878.2:n.2190+222_2190+224delinsGAC
XM_005252822.4:c.2157+222_2157+224delinsGAC	XP_005252879.1:n.2157+222_2157+224delinsGAC
XM_011519949.2:c.2142+222_2142+224delinsGAC	XP_011518251.1:n.2142+222_2142+224delinsGAC
NM_001142649.2:c.2232+222_2232+224delinsGAC	NP_001136121.1:n.2232+222_2232+224delinsGAC
NM_213599.3:c.2235+222_2235+224delinsGAC MANE Select	NP_998764.1:n.2235+222_2235+224delinsGAC