Canonical Allele Identifier: CA5923313

Gene: ANO5

Linked Data

• dbSNP Id: rs753573665
• ExAC: 11:22283664 TAA / T
• gnomAD v2: 11-22283664-TAA-T
• gnomAD v3: 11-22262118-TAA-T
• MyVariant Identifiers: chr11:g.22283665_22283666del (hg19) ; chr11:g.22262119_22262120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262119_22262120del , CM000673.2:g.22262119_22262120del	GRCh38
NC_000011.9:g.22283665_22283666del , CM000673.1:g.22283665_22283666del	GRCh37
NC_000011.8:g.22240241_22240242del	NCBI36
NG_015844.1:g.73944_73945del , LRG_868:g.73944_73945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1181-10_1181-9del	ENSP00000507766.1:n.1181-10_1181-9del
ENST00000682341.1:c.1589-10_1589-9del	ENSP00000508251.1:n.1589-10_1589-9del
ENST00000683197.1:c.1589-10_1589-9del	ENSP00000507641.1:n.1589-10_1589-9del
ENST00000683411.1:c.1181-10_1181-9del	ENSP00000508397.1:n.1181-10_1181-9del
ENST00000683437.1:c.1181-10_1181-9del	ENSP00000508408.1:n.1181-10_1181-9del
ENST00000683613.1:n.2625-10_2625-9del
ENST00000684663.1:c.1586-10_1586-9del	ENSP00000508009.1:n.1586-10_1586-9del
ENST00000324559.9:c.1631-10_1631-9del MANE Select	ENSP00000315371.9:n.1631-10_1631-9del
ENST00000648804.1:n.1966-10_1966-9del
ENST00000324559.8:c.1631-10_1631-9del	ENSP00000315371.8:n.1631-10_1631-9del
NM_001142649.1:c.1628-10_1628-9del	NP_001136121.1:n.1628-10_1628-9del
NM_213599.2:c.1631-10_1631-9del , LRG_868t1:c.1631-10_1631-9del	NP_998764.1:n.1631-10_1631-9del
XM_005252820.2:c.1589-10_1589-9del	XP_005252877.2:n.1589-10_1589-9del
XM_005252821.2:c.1586-10_1586-9del	XP_005252878.2:n.1586-10_1586-9del
XM_005252822.3:c.1553-10_1553-9del	XP_005252879.1:n.1553-10_1553-9del
XM_005252823.3:c.1550-10_1550-9del	XP_005252880.1:n.1550-10_1550-9del
XM_011519949.1:c.1538-10_1538-9del	XP_011518251.1:n.1538-10_1538-9del
XM_005252820.3:c.1589-10_1589-9del	XP_005252877.2:n.1589-10_1589-9del
XM_005252821.3:c.1586-10_1586-9del	XP_005252878.2:n.1586-10_1586-9del
XM_005252822.4:c.1553-10_1553-9del	XP_005252879.1:n.1553-10_1553-9del
XM_011519949.2:c.1538-10_1538-9del	XP_011518251.1:n.1538-10_1538-9del
NM_001142649.2:c.1628-10_1628-9del	NP_001136121.1:n.1628-10_1628-9del
NM_213599.3:c.1631-10_1631-9del MANE Select	NP_998764.1:n.1631-10_1631-9del