Canonical Allele Identifier: CA379922103

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281131G>A (hg19) ; chr11:g.22259585G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259585G>A , CM000673.2:g.22259585G>A	GRCh38
NC_000011.9:g.22281131G>A , CM000673.1:g.22281131G>A	GRCh37
NC_000011.8:g.22237707G>A	NCBI36
NG_015844.1:g.71410G>A , LRG_868:g.71410G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1024G>A	ENSP00000507766.1:p.Ala342Thr
ENST00000682341.1:c.1432G>A	ENSP00000508251.1:p.Ala478Thr
ENST00000683197.1:c.1432G>A	ENSP00000507641.1:p.Ala478Thr
ENST00000683411.1:c.1024G>A	ENSP00000508397.1:p.Ala342Thr
ENST00000683437.1:c.1024G>A	ENSP00000508408.1:p.Ala342Thr
ENST00000683613.1:n.2468G>A
ENST00000684663.1:c.1429G>A	ENSP00000508009.1:p.Ala477Thr
ENST00000324559.9:c.1474G>A MANE Select	ENSP00000315371.9:p.Ala492Thr
ENST00000648804.1:n.1809G>A
ENST00000324559.8:c.1474G>A	ENSP00000315371.8:p.Ala492Thr
NM_001142649.1:c.1471G>A	NP_001136121.1:p.Ala491Thr
NM_213599.2:c.1474G>A , LRG_868t1:c.1474G>A	NP_998764.1:p.Ala492Thr
XM_005252820.2:c.1432G>A	XP_005252877.2:p.Ala478Thr
XM_005252821.2:c.1429G>A	XP_005252878.2:p.Ala477Thr
XM_005252822.3:c.1396G>A	XP_005252879.1:p.Ala466Thr
XM_005252823.3:c.1393G>A	XP_005252880.1:p.Ala465Thr
XM_011519949.1:c.1381G>A	XP_011518251.1:p.Ala461Thr
XM_005252820.3:c.1432G>A	XP_005252877.2:p.Ala478Thr
XM_005252821.3:c.1429G>A	XP_005252878.2:p.Ala477Thr
XM_005252822.4:c.1396G>A	XP_005252879.1:p.Ala466Thr
XM_011519949.2:c.1381G>A	XP_011518251.1:p.Ala461Thr
NM_001142649.2:c.1471G>A	NP_001136121.1:p.Ala491Thr
NM_213599.3:c.1474G>A MANE Select	NP_998764.1:p.Ala492Thr