Canonical Allele Identifier: CA379923357

Gene: ANO5

Linked Data

• gnomAD v4: 11-22270376-T-A
• MyVariant Identifiers: chr11:g.22291922T>A (hg19) ; chr11:g.22270376T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22270376T>A , CM000673.2:g.22270376T>A	GRCh38
NC_000011.9:g.22291922T>A , CM000673.1:g.22291922T>A	GRCh37
NC_000011.8:g.22248498T>A	NCBI36
NG_015844.1:g.82201T>A , LRG_868:g.82201T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1513T>A	ENSP00000507766.1:p.Trp505Arg
ENST00000682341.1:c.1921T>A	ENSP00000508251.1:p.Trp641Arg
ENST00000683197.1:c.1921T>A	ENSP00000507641.1:p.Trp641Arg
ENST00000683411.1:c.1513T>A	ENSP00000508397.1:p.Trp505Arg
ENST00000683437.1:c.1513T>A	ENSP00000508408.1:p.Trp505Arg
ENST00000683613.1:n.2957T>A
ENST00000684663.1:c.1918T>A	ENSP00000508009.1:p.Trp640Arg
ENST00000324559.9:c.1963T>A MANE Select	ENSP00000315371.9:p.Trp655Arg
ENST00000648804.1:n.2298T>A
ENST00000324559.8:c.1963T>A	ENSP00000315371.8:p.Trp655Arg
NM_001142649.1:c.1960T>A	NP_001136121.1:p.Trp654Arg
NM_213599.2:c.1963T>A , LRG_868t1:c.1963T>A	NP_998764.1:p.Trp655Arg
XM_005252820.2:c.1921T>A	XP_005252877.2:p.Trp641Arg
XM_005252821.2:c.1918T>A	XP_005252878.2:p.Trp640Arg
XM_005252822.3:c.1885T>A	XP_005252879.1:p.Trp629Arg
XM_005252823.3:c.1882T>A	XP_005252880.1:p.Trp628Arg
XM_011519949.1:c.1870T>A	XP_011518251.1:p.Trp624Arg
XM_005252820.3:c.1921T>A	XP_005252877.2:p.Trp641Arg
XM_005252821.3:c.1918T>A	XP_005252878.2:p.Trp640Arg
XM_005252822.4:c.1885T>A	XP_005252879.1:p.Trp629Arg
XM_011519949.2:c.1870T>A	XP_011518251.1:p.Trp624Arg
NM_001142649.2:c.1960T>A	NP_001136121.1:p.Trp654Arg
NM_213599.3:c.1963T>A MANE Select	NP_998764.1:p.Trp655Arg