Canonical Allele Identifier: CA473404187

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271897A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250351A>C , CM000673.2:g.22250351A>C	GRCh38
NC_000011.9:g.22271897A>C , CM000673.1:g.22271897A>C	GRCh37
NC_000011.8:g.22228473A>C	NCBI36
NG_015844.1:g.62176A>C , LRG_868:g.62176A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.313A>C
ENST00000682266.1:c.543A>C	ENSP00000507766.1:p.Ser181=
ENST00000682341.1:c.951A>C	ENSP00000508251.1:p.Ser317=
ENST00000682530.1:c.*925A>C	ENSP00000506805.1:n.*925A>C
ENST00000683197.1:c.951A>C	ENSP00000507641.1:p.Ser317=
ENST00000683411.1:c.543A>C	ENSP00000508397.1:p.Ser181=
ENST00000683437.1:c.543A>C	ENSP00000508408.1:p.Ser181=
ENST00000683613.1:n.1987A>C
ENST00000683834.1:n.1193A>C
ENST00000684663.1:c.948A>C	ENSP00000508009.1:p.Ser316=
ENST00000324559.9:c.993A>C MANE Select	ENSP00000315371.9:p.Ser331=
ENST00000648804.1:n.1328A>C
ENST00000324559.8:c.993A>C	ENSP00000315371.8:p.Ser331=
NM_001142649.1:c.990A>C	NP_001136121.1:p.Ser330=
NM_213599.2:c.993A>C , LRG_868t1:c.993A>C	NP_998764.1:p.Ser331=
XM_005252820.2:c.951A>C	XP_005252877.2:p.Ser317=
XM_005252821.2:c.948A>C	XP_005252878.2:p.Ser316=
XM_005252822.3:c.915A>C	XP_005252879.1:p.Ser305=
XM_005252823.3:c.912A>C	XP_005252880.1:p.Ser304=
XM_011519949.1:c.900A>C	XP_011518251.1:p.Ser300=
XM_005252820.3:c.951A>C	XP_005252877.2:p.Ser317=
XM_005252821.3:c.948A>C	XP_005252878.2:p.Ser316=
XM_005252822.4:c.915A>C	XP_005252879.1:p.Ser305=
XM_011519949.2:c.900A>C	XP_011518251.1:p.Ser300=
NM_001142649.2:c.990A>C	NP_001136121.1:p.Ser330=
NM_213599.3:c.993A>C MANE Select	NP_998764.1:p.Ser331=