Canonical Allele Identifier: CA598389497

Gene: ANO5

Linked Data

• dbSNP Id: rs1402491477
• gnomAD v2: 11-22294794-ATAAG-A
• gnomAD v3: 11-22273248-ATAAG-A
• gnomAD v4: 11-22273248-ATAAG-A
• MyVariant Identifiers: chr11:g.22294795_22294798del (hg19) ; chr11:g.22273249_22273252del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22273252_22273255del , CM000673.2:g.22273252_22273255del	GRCh38
NC_000011.9:g.22294798_22294801del , CM000673.1:g.22294798_22294801del	GRCh37
NC_000011.8:g.22251374_22251377del	NCBI36
NG_015844.1:g.85077_85080del , LRG_868:g.85077_85080del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.252+263_252+266del
ENST00000682266.1:c.1785+263_1785+266del	ENSP00000507766.1:n.1785+263_1785+266del
ENST00000682341.1:c.2193+263_2193+266del	ENSP00000508251.1:n.2193+263_2193+266del
ENST00000683197.1:c.2193+263_2193+266del	ENSP00000507641.1:n.2193+263_2193+266del
ENST00000683411.1:c.1785+263_1785+266del	ENSP00000508397.1:n.1785+263_1785+266del
ENST00000683437.1:c.1785+263_1785+266del	ENSP00000508408.1:n.1785+263_1785+266del
ENST00000683613.1:n.3229+263_3229+266del
ENST00000684663.1:c.2190+263_2190+266del	ENSP00000508009.1:n.2190+263_2190+266del
ENST00000324559.9:c.2235+263_2235+266del MANE Select	ENSP00000315371.9:n.2235+263_2235+266del
ENST00000648804.1:n.2570+263_2570+266del
ENST00000324559.8:c.2235+263_2235+266del	ENSP00000315371.8:n.2235+263_2235+266del
ENST00000532043.1:n.252+263_252+266del
NM_001142649.1:c.2232+263_2232+266del	NP_001136121.1:n.2232+263_2232+266del
NM_213599.2:c.2235+263_2235+266del , LRG_868t1:c.2235+263_2235+266del	NP_998764.1:n.2235+263_2235+266del
XM_005252820.2:c.2193+263_2193+266del	XP_005252877.2:n.2193+263_2193+266del
XM_005252821.2:c.2190+263_2190+266del	XP_005252878.2:n.2190+263_2190+266del
XM_005252822.3:c.2157+263_2157+266del	XP_005252879.1:n.2157+263_2157+266del
XM_005252823.3:c.2154+263_2154+266del	XP_005252880.1:n.2154+263_2154+266del
XM_011519949.1:c.2142+263_2142+266del	XP_011518251.1:n.2142+263_2142+266del
XM_005252820.3:c.2193+263_2193+266del	XP_005252877.2:n.2193+263_2193+266del
XM_005252821.3:c.2190+263_2190+266del	XP_005252878.2:n.2190+263_2190+266del
XM_005252822.4:c.2157+263_2157+266del	XP_005252879.1:n.2157+263_2157+266del
XM_011519949.2:c.2142+263_2142+266del	XP_011518251.1:n.2142+263_2142+266del
NM_001142649.2:c.2232+263_2232+266del	NP_001136121.1:n.2232+263_2232+266del
NM_213599.3:c.2235+263_2235+266del MANE Select	NP_998764.1:n.2235+263_2235+266del