Canonical Allele Identifier: CA379923245

Gene: ANO5

Linked Data

• dbSNP Id: rs2133778212
• gnomAD v3: 11-22270322-A-G
• gnomAD v4: 11-22270322-A-G
• MyVariant Identifiers: chr11:g.22291868A>G (hg19) ; chr11:g.22270322A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22270322A>G , CM000673.2:g.22270322A>G	GRCh38
NC_000011.9:g.22291868A>G , CM000673.1:g.22291868A>G	GRCh37
NC_000011.8:g.22248444A>G	NCBI36
NG_015844.1:g.82147A>G , LRG_868:g.82147A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1459A>G	ENSP00000507766.1:p.Asn487Asp
ENST00000682341.1:c.1867A>G	ENSP00000508251.1:p.Asn623Asp
ENST00000683197.1:c.1867A>G	ENSP00000507641.1:p.Asn623Asp
ENST00000683411.1:c.1459A>G	ENSP00000508397.1:p.Asn487Asp
ENST00000683437.1:c.1459A>G	ENSP00000508408.1:p.Asn487Asp
ENST00000683613.1:n.2903A>G
ENST00000684663.1:c.1864A>G	ENSP00000508009.1:p.Asn622Asp
ENST00000324559.9:c.1909A>G MANE Select	ENSP00000315371.9:p.Asn637Asp
ENST00000648804.1:n.2244A>G
ENST00000324559.8:c.1909A>G	ENSP00000315371.8:p.Asn637Asp
NM_001142649.1:c.1906A>G	NP_001136121.1:p.Asn636Asp
NM_213599.2:c.1909A>G , LRG_868t1:c.1909A>G	NP_998764.1:p.Asn637Asp
XM_005252820.2:c.1867A>G	XP_005252877.2:p.Asn623Asp
XM_005252821.2:c.1864A>G	XP_005252878.2:p.Asn622Asp
XM_005252822.3:c.1831A>G	XP_005252879.1:p.Asn611Asp
XM_005252823.3:c.1828A>G	XP_005252880.1:p.Asn610Asp
XM_011519949.1:c.1816A>G	XP_011518251.1:p.Asn606Asp
XM_005252820.3:c.1867A>G	XP_005252877.2:p.Asn623Asp
XM_005252821.3:c.1864A>G	XP_005252878.2:p.Asn622Asp
XM_005252822.4:c.1831A>G	XP_005252879.1:p.Asn611Asp
XM_011519949.2:c.1816A>G	XP_011518251.1:p.Asn606Asp
NM_001142649.2:c.1906A>G	NP_001136121.1:p.Asn636Asp
NM_213599.3:c.1909A>G MANE Select	NP_998764.1:p.Asn637Asp