Canonical Allele Identifier: CA379922489

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22283686A>G (hg19) ; chr11:g.22262140A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262140A>G , CM000673.2:g.22262140A>G	GRCh38
NC_000011.9:g.22283686A>G , CM000673.1:g.22283686A>G	GRCh37
NC_000011.8:g.22240262A>G	NCBI36
NG_015844.1:g.73965A>G , LRG_868:g.73965A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1192A>G	ENSP00000507766.1:p.Thr398Ala
ENST00000682341.1:c.1600A>G	ENSP00000508251.1:p.Thr534Ala
ENST00000683197.1:c.1600A>G	ENSP00000507641.1:p.Thr534Ala
ENST00000683411.1:c.1192A>G	ENSP00000508397.1:p.Thr398Ala
ENST00000683437.1:c.1192A>G	ENSP00000508408.1:p.Thr398Ala
ENST00000683613.1:n.2636A>G
ENST00000684663.1:c.1597A>G	ENSP00000508009.1:p.Thr533Ala
ENST00000324559.9:c.1642A>G MANE Select	ENSP00000315371.9:p.Thr548Ala
ENST00000648804.1:n.1977A>G
ENST00000324559.8:c.1642A>G	ENSP00000315371.8:p.Thr548Ala
NM_001142649.1:c.1639A>G	NP_001136121.1:p.Thr547Ala
NM_213599.2:c.1642A>G , LRG_868t1:c.1642A>G	NP_998764.1:p.Thr548Ala
XM_005252820.2:c.1600A>G	XP_005252877.2:p.Thr534Ala
XM_005252821.2:c.1597A>G	XP_005252878.2:p.Thr533Ala
XM_005252822.3:c.1564A>G	XP_005252879.1:p.Thr522Ala
XM_005252823.3:c.1561A>G	XP_005252880.1:p.Thr521Ala
XM_011519949.1:c.1549A>G	XP_011518251.1:p.Thr517Ala
XM_005252820.3:c.1600A>G	XP_005252877.2:p.Thr534Ala
XM_005252821.3:c.1597A>G	XP_005252878.2:p.Thr533Ala
XM_005252822.4:c.1564A>G	XP_005252879.1:p.Thr522Ala
XM_011519949.2:c.1549A>G	XP_011518251.1:p.Thr517Ala
NM_001142649.2:c.1639A>G	NP_001136121.1:p.Thr547Ala
NM_213599.3:c.1642A>G MANE Select	NP_998764.1:p.Thr548Ala