Canonical Allele Identifier: CA379922208

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281176T>A (hg19) ; chr11:g.22259630T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259630T>A , CM000673.2:g.22259630T>A	GRCh38
NC_000011.9:g.22281176T>A , CM000673.1:g.22281176T>A	GRCh37
NC_000011.8:g.22237752T>A	NCBI36
NG_015844.1:g.71455T>A , LRG_868:g.71455T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1069T>A	ENSP00000507766.1:p.Phe357Ile
ENST00000682341.1:c.1477T>A	ENSP00000508251.1:p.Phe493Ile
ENST00000683197.1:c.1477T>A	ENSP00000507641.1:p.Phe493Ile
ENST00000683411.1:c.1069T>A	ENSP00000508397.1:p.Phe357Ile
ENST00000683437.1:c.1069T>A	ENSP00000508408.1:p.Phe357Ile
ENST00000683613.1:n.2513T>A
ENST00000684663.1:c.1474T>A	ENSP00000508009.1:p.Phe492Ile
ENST00000324559.9:c.1519T>A MANE Select	ENSP00000315371.9:p.Phe507Ile
ENST00000648804.1:n.1854T>A
ENST00000324559.8:c.1519T>A	ENSP00000315371.8:p.Phe507Ile
NM_001142649.1:c.1516T>A	NP_001136121.1:p.Phe506Ile
NM_213599.2:c.1519T>A , LRG_868t1:c.1519T>A	NP_998764.1:p.Phe507Ile
XM_005252820.2:c.1477T>A	XP_005252877.2:p.Phe493Ile
XM_005252821.2:c.1474T>A	XP_005252878.2:p.Phe492Ile
XM_005252822.3:c.1441T>A	XP_005252879.1:p.Phe481Ile
XM_005252823.3:c.1438T>A	XP_005252880.1:p.Phe480Ile
XM_011519949.1:c.1426T>A	XP_011518251.1:p.Phe476Ile
XM_005252820.3:c.1477T>A	XP_005252877.2:p.Phe493Ile
XM_005252821.3:c.1474T>A	XP_005252878.2:p.Phe492Ile
XM_005252822.4:c.1441T>A	XP_005252879.1:p.Phe481Ile
XM_011519949.2:c.1426T>A	XP_011518251.1:p.Phe476Ile
NM_001142649.2:c.1516T>A	NP_001136121.1:p.Phe506Ile
NM_213599.3:c.1519T>A MANE Select	NP_998764.1:p.Phe507Ile