Canonical Allele Identifier: CA1957413245

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250352A= , CM000673.2:g.22250352A=	GRCh38
NC_000011.9:g.22271898A= , CM000673.1:g.22271898A=	GRCh37
NC_000011.8:g.22228474A=	NCBI36
NG_015844.1:g.62177A= , LRG_868:g.62177A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.314A=
ENST00000682266.1:c.544A=	ENSP00000507766.1:p.Met182=
ENST00000682341.1:c.952A=	ENSP00000508251.1:p.Met318=
ENST00000682530.1:c.*926A=	ENSP00000506805.1:n.*926A=
ENST00000683197.1:c.952A=	ENSP00000507641.1:p.Met318=
ENST00000683411.1:c.544A=	ENSP00000508397.1:p.Met182=
ENST00000683437.1:c.544A=	ENSP00000508408.1:p.Met182=
ENST00000683613.1:n.1988A=
ENST00000683834.1:n.1194A=
ENST00000684663.1:c.949A=	ENSP00000508009.1:p.Met317=
ENST00000324559.9:c.994A= MANE Select	ENSP00000315371.9:p.Met332=
ENST00000648804.1:n.1329A=
ENST00000324559.8:c.994A=	ENSP00000315371.8:p.Met332=
NM_001142649.1:c.991A=	NP_001136121.1:p.Met331=
NM_213599.2:c.994A= , LRG_868t1:c.994A=	NP_998764.1:p.Met332=
XM_005252820.2:c.952A=	XP_005252877.2:p.Met318=
XM_005252821.2:c.949A=	XP_005252878.2:p.Met317=
XM_005252822.3:c.916A=	XP_005252879.1:p.Met306=
XM_005252823.3:c.913A=	XP_005252880.1:p.Met305=
XM_011519949.1:c.901A=	XP_011518251.1:p.Met301=
XM_005252820.3:c.952A=	XP_005252877.2:p.Met318=
XM_005252821.3:c.949A=	XP_005252878.2:p.Met317=
XM_005252822.4:c.916A=	XP_005252879.1:p.Met306=
XM_011519949.2:c.901A=	XP_011518251.1:p.Met301=
NM_001142649.2:c.991A=	NP_001136121.1:p.Met331=
NM_213599.3:c.994A= MANE Select	NP_998764.1:p.Met332=