Canonical Allele Identifier: CA1957403598

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22273248_22273252delinsATAAG , CM000673.2:g.22273248_22273252delinsATAAG	GRCh38
NC_000011.9:g.22294794_22294798delinsATAAG , CM000673.1:g.22294794_22294798delinsATAAG	GRCh37
NC_000011.8:g.22251370_22251374delinsATAAG	NCBI36
NG_015844.1:g.85073_85077delinsATAAG , LRG_868:g.85073_85077delinsATAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.252+259_252+263delinsATAAG
ENST00000682266.1:c.1785+259_1785+263delinsATAAG	ENSP00000507766.1:n.1785+259_1785+263delinsATAAG
ENST00000682341.1:c.2193+259_2193+263delinsATAAG	ENSP00000508251.1:n.2193+259_2193+263delinsATAAG
ENST00000683197.1:c.2193+259_2193+263delinsATAAG	ENSP00000507641.1:n.2193+259_2193+263delinsATAAG
ENST00000683411.1:c.1785+259_1785+263delinsATAAG	ENSP00000508397.1:n.1785+259_1785+263delinsATAAG
ENST00000683437.1:c.1785+259_1785+263delinsATAAG	ENSP00000508408.1:n.1785+259_1785+263delinsATAAG
ENST00000683613.1:n.3229+259_3229+263delinsATAAG
ENST00000684663.1:c.2190+259_2190+263delinsATAAG	ENSP00000508009.1:n.2190+259_2190+263delinsATAAG
ENST00000324559.9:c.2235+259_2235+263delinsATAAG MANE Select	ENSP00000315371.9:n.2235+259_2235+263delinsATAAG
ENST00000648804.1:n.2570+259_2570+263delinsATAAG
ENST00000324559.8:c.2235+259_2235+263delinsATAAG	ENSP00000315371.8:n.2235+259_2235+263delinsATAAG
ENST00000532043.1:n.252+259_252+263delinsATAAG
NM_001142649.1:c.2232+259_2232+263delinsATAAG	NP_001136121.1:n.2232+259_2232+263delinsATAAG
NM_213599.2:c.2235+259_2235+263delinsATAAG , LRG_868t1:c.2235+259_2235+263delinsATAAG	NP_998764.1:n.2235+259_2235+263delinsATAAG
XM_005252820.2:c.2193+259_2193+263delinsATAAG	XP_005252877.2:n.2193+259_2193+263delinsATAAG
XM_005252821.2:c.2190+259_2190+263delinsATAAG	XP_005252878.2:n.2190+259_2190+263delinsATAAG
XM_005252822.3:c.2157+259_2157+263delinsATAAG	XP_005252879.1:n.2157+259_2157+263delinsATAAG
XM_005252823.3:c.2154+259_2154+263delinsATAAG	XP_005252880.1:n.2154+259_2154+263delinsATAAG
XM_011519949.1:c.2142+259_2142+263delinsATAAG	XP_011518251.1:n.2142+259_2142+263delinsATAAG
XM_005252820.3:c.2193+259_2193+263delinsATAAG	XP_005252877.2:n.2193+259_2193+263delinsATAAG
XM_005252821.3:c.2190+259_2190+263delinsATAAG	XP_005252878.2:n.2190+259_2190+263delinsATAAG
XM_005252822.4:c.2157+259_2157+263delinsATAAG	XP_005252879.1:n.2157+259_2157+263delinsATAAG
XM_011519949.2:c.2142+259_2142+263delinsATAAG	XP_011518251.1:n.2142+259_2142+263delinsATAAG
NM_001142649.2:c.2232+259_2232+263delinsATAAG	NP_001136121.1:n.2232+259_2232+263delinsATAAG
NM_213599.3:c.2235+259_2235+263delinsATAAG MANE Select	NP_998764.1:n.2235+259_2235+263delinsATAAG