Canonical Allele Identifier: CA218774896

Gene: ANO5

Linked Data

• dbSNP Id: rs766878815
• MyVariant Identifiers: chr11:g.22242654T>A (hg19) ; chr11:g.22221108T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221108T>A , CM000673.2:g.22221108T>A	GRCh38
NC_000011.9:g.22242654T>A , CM000673.1:g.22242654T>A	GRCh37
NC_000011.8:g.22199230T>A	NCBI36
NG_015844.1:g.32933T>A , LRG_868:g.32933T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.-259T>A	ENSP00000507766.1:n.-259T>A
ENST00000682341.1:c.150T>A	ENSP00000508251.1:p.Asn50Lys
ENST00000682530.1:c.*124T>A	ENSP00000506805.1:n.*124T>A
ENST00000682684.1:n.571T>A
ENST00000683197.1:c.150T>A	ENSP00000507641.1:p.Asn50Lys
ENST00000683411.1:c.-259T>A	ENSP00000508397.1:n.-259T>A
ENST00000683437.1:c.-259T>A	ENSP00000508408.1:n.-259T>A
ENST00000683613.1:n.1186T>A
ENST00000683834.1:n.392T>A
ENST00000683897.1:n.436T>A
ENST00000684365.1:n.561T>A
ENST00000684663.1:c.147T>A	ENSP00000508009.1:p.Asn49Lys
ENST00000324559.9:c.192T>A MANE Select	ENSP00000315371.9:p.Asn64Lys
ENST00000648804.1:n.757T>A
ENST00000324559.8:c.192T>A	ENSP00000315371.8:p.Asn64Lys
NM_001142649.1:c.189T>A	NP_001136121.1:p.Asn63Lys
NM_213599.2:c.192T>A , LRG_868t1:c.192T>A	NP_998764.1:p.Asn64Lys
XM_005252820.2:c.150T>A	XP_005252877.2:p.Asn50Lys
XM_005252821.2:c.147T>A	XP_005252878.2:p.Asn49Lys
XM_005252822.3:c.114T>A	XP_005252879.1:p.Asn38Lys
XM_005252823.3:c.111T>A	XP_005252880.1:p.Asn37Lys
XM_011519949.1:c.99T>A	XP_011518251.1:p.Asn33Lys
XM_005252820.3:c.150T>A	XP_005252877.2:p.Asn50Lys
XM_005252821.3:c.147T>A	XP_005252878.2:p.Asn49Lys
XM_005252822.4:c.114T>A	XP_005252879.1:p.Asn38Lys
XM_011519949.2:c.99T>A	XP_011518251.1:p.Asn33Lys
NM_001142649.2:c.189T>A	NP_001136121.1:p.Asn63Lys
NM_213599.3:c.192T>A MANE Select	NP_998764.1:p.Asn64Lys