Canonical Allele Identifier: CA379925181

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22242663C>G (hg19) ; chr11:g.22221117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221117C>G , CM000673.2:g.22221117C>G	GRCh38
NC_000011.9:g.22242663C>G , CM000673.1:g.22242663C>G	GRCh37
NC_000011.8:g.22199239C>G	NCBI36
NG_015844.1:g.32942C>G , LRG_868:g.32942C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.-250C>G	ENSP00000507766.1:n.-250C>G
ENST00000682341.1:c.159C>G	ENSP00000508251.1:p.Ser53Arg
ENST00000682530.1:c.*133C>G	ENSP00000506805.1:n.*133C>G
ENST00000682684.1:n.580C>G
ENST00000683197.1:c.159C>G	ENSP00000507641.1:p.Ser53Arg
ENST00000683411.1:c.-250C>G	ENSP00000508397.1:n.-250C>G
ENST00000683437.1:c.-250C>G	ENSP00000508408.1:n.-250C>G
ENST00000683613.1:n.1195C>G
ENST00000683834.1:n.401C>G
ENST00000683897.1:n.445C>G
ENST00000684365.1:n.570C>G
ENST00000684663.1:c.156C>G	ENSP00000508009.1:p.Ser52Arg
ENST00000324559.9:c.201C>G MANE Select	ENSP00000315371.9:p.Ser67Arg
ENST00000648804.1:n.766C>G
ENST00000324559.8:c.201C>G	ENSP00000315371.8:p.Ser67Arg
NM_001142649.1:c.198C>G	NP_001136121.1:p.Ser66Arg
NM_213599.2:c.201C>G , LRG_868t1:c.201C>G	NP_998764.1:p.Ser67Arg
XM_005252820.2:c.159C>G	XP_005252877.2:p.Ser53Arg
XM_005252821.2:c.156C>G	XP_005252878.2:p.Ser52Arg
XM_005252822.3:c.123C>G	XP_005252879.1:p.Ser41Arg
XM_005252823.3:c.120C>G	XP_005252880.1:p.Ser40Arg
XM_011519949.1:c.108C>G	XP_011518251.1:p.Ser36Arg
XM_005252820.3:c.159C>G	XP_005252877.2:p.Ser53Arg
XM_005252821.3:c.156C>G	XP_005252878.2:p.Ser52Arg
XM_005252822.4:c.123C>G	XP_005252879.1:p.Ser41Arg
XM_011519949.2:c.108C>G	XP_011518251.1:p.Ser36Arg
NM_001142649.2:c.198C>G	NP_001136121.1:p.Ser66Arg
NM_213599.3:c.201C>G MANE Select	NP_998764.1:p.Ser67Arg