Canonical Allele Identifier: CA1957413249

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250354G= , CM000673.2:g.22250354G=	GRCh38
NC_000011.9:g.22271900G= , CM000673.1:g.22271900G=	GRCh37
NC_000011.8:g.22228476G=	NCBI36
NG_015844.1:g.62179G= , LRG_868:g.62179G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.316G=
ENST00000682266.1:c.546G=	ENSP00000507766.1:p.Met182=
ENST00000682341.1:c.954G=	ENSP00000508251.1:p.Met318=
ENST00000682530.1:c.*928G=	ENSP00000506805.1:n.*928G=
ENST00000683197.1:c.954G=	ENSP00000507641.1:p.Met318=
ENST00000683411.1:c.546G=	ENSP00000508397.1:p.Met182=
ENST00000683437.1:c.546G=	ENSP00000508408.1:p.Met182=
ENST00000683613.1:n.1990G=
ENST00000683834.1:n.1196G=
ENST00000684663.1:c.951G=	ENSP00000508009.1:p.Met317=
ENST00000324559.9:c.996G= MANE Select	ENSP00000315371.9:p.Met332=
ENST00000648804.1:n.1331G=
ENST00000324559.8:c.996G=	ENSP00000315371.8:p.Met332=
NM_001142649.1:c.993G=	NP_001136121.1:p.Met331=
NM_213599.2:c.996G= , LRG_868t1:c.996G=	NP_998764.1:p.Met332=
XM_005252820.2:c.954G=	XP_005252877.2:p.Met318=
XM_005252821.2:c.951G=	XP_005252878.2:p.Met317=
XM_005252822.3:c.918G=	XP_005252879.1:p.Met306=
XM_005252823.3:c.915G=	XP_005252880.1:p.Met305=
XM_011519949.1:c.903G=	XP_011518251.1:p.Met301=
XM_005252820.3:c.954G=	XP_005252877.2:p.Met318=
XM_005252821.3:c.951G=	XP_005252878.2:p.Met317=
XM_005252822.4:c.918G=	XP_005252879.1:p.Met306=
XM_011519949.2:c.903G=	XP_011518251.1:p.Met301=
NM_001142649.2:c.993G=	NP_001136121.1:p.Met331=
NM_213599.3:c.996G= MANE Select	NP_998764.1:p.Met332=