Canonical Allele Identifier: CA473402393

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22257726A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22236180A>T , CM000673.2:g.22236180A>T	GRCh38
NC_000011.9:g.22257726A>T , CM000673.1:g.22257726A>T	GRCh37
NC_000011.8:g.22214302A>T	NCBI36
NG_015844.1:g.48005A>T , LRG_868:g.48005A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.216A>T	ENSP00000507766.1:p.Ser72=
ENST00000682341.1:c.624A>T	ENSP00000508251.1:p.Ser208=
ENST00000682530.1:c.*598A>T	ENSP00000506805.1:n.*598A>T
ENST00000682684.1:n.1045A>T
ENST00000683197.1:c.624A>T	ENSP00000507641.1:p.Ser208=
ENST00000683411.1:c.216A>T	ENSP00000508397.1:p.Ser72=
ENST00000683437.1:c.216A>T	ENSP00000508408.1:p.Ser72=
ENST00000683613.1:n.1660A>T
ENST00000683834.1:n.866A>T
ENST00000684663.1:c.621A>T	ENSP00000508009.1:p.Ser207=
ENST00000324559.9:c.666A>T MANE Select	ENSP00000315371.9:p.Ser222=
ENST00000648804.1:n.1213+8594A>T
ENST00000324559.8:c.666A>T	ENSP00000315371.8:p.Ser222=
NM_001142649.1:c.663A>T	NP_001136121.1:p.Ser221=
NM_213599.2:c.666A>T , LRG_868t1:c.666A>T	NP_998764.1:p.Ser222=
XM_005252820.2:c.624A>T	XP_005252877.2:p.Ser208=
XM_005252821.2:c.621A>T	XP_005252878.2:p.Ser207=
XM_005252822.3:c.588A>T	XP_005252879.1:p.Ser196=
XM_005252823.3:c.585A>T	XP_005252880.1:p.Ser195=
XM_011519949.1:c.573A>T	XP_011518251.1:p.Ser191=
XM_005252820.3:c.624A>T	XP_005252877.2:p.Ser208=
XM_005252821.3:c.621A>T	XP_005252878.2:p.Ser207=
XM_005252822.4:c.588A>T	XP_005252879.1:p.Ser196=
XM_011519949.2:c.573A>T	XP_011518251.1:p.Ser191=
NM_001142649.2:c.663A>T	NP_001136121.1:p.Ser221=
NM_213599.3:c.666A>T MANE Select	NP_998764.1:p.Ser222=