Canonical Allele Identifier: CA1957413251

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250361A= , CM000673.2:g.22250361A=	GRCh38
NC_000011.9:g.22271907A= , CM000673.1:g.22271907A=	GRCh37
NC_000011.8:g.22228483A=	NCBI36
NG_015844.1:g.62186A= , LRG_868:g.62186A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.323A=
ENST00000682266.1:c.553A=	ENSP00000507766.1:p.Asn185=
ENST00000682341.1:c.961A=	ENSP00000508251.1:p.Asn321=
ENST00000682530.1:c.*935A=	ENSP00000506805.1:n.*935A=
ENST00000683197.1:c.961A=	ENSP00000507641.1:p.Asn321=
ENST00000683411.1:c.553A=	ENSP00000508397.1:p.Asn185=
ENST00000683437.1:c.553A=	ENSP00000508408.1:p.Asn185=
ENST00000683613.1:n.1997A=
ENST00000683834.1:n.1203A=
ENST00000684663.1:c.958A=	ENSP00000508009.1:p.Asn320=
ENST00000324559.9:c.1003A= MANE Select	ENSP00000315371.9:p.Asn335=
ENST00000648804.1:n.1338A=
ENST00000324559.8:c.1003A=	ENSP00000315371.8:p.Asn335=
NM_001142649.1:c.1000A=	NP_001136121.1:p.Asn334=
NM_213599.2:c.1003A= , LRG_868t1:c.1003A=	NP_998764.1:p.Asn335=
XM_005252820.2:c.961A=	XP_005252877.2:p.Asn321=
XM_005252821.2:c.958A=	XP_005252878.2:p.Asn320=
XM_005252822.3:c.925A=	XP_005252879.1:p.Asn309=
XM_005252823.3:c.922A=	XP_005252880.1:p.Asn308=
XM_011519949.1:c.910A=	XP_011518251.1:p.Asn304=
XM_005252820.3:c.961A=	XP_005252877.2:p.Asn321=
XM_005252821.3:c.958A=	XP_005252878.2:p.Asn320=
XM_005252822.4:c.925A=	XP_005252879.1:p.Asn309=
XM_011519949.2:c.910A=	XP_011518251.1:p.Asn304=
NM_001142649.2:c.1000A=	NP_001136121.1:p.Asn334=
NM_213599.3:c.1003A= MANE Select	NP_998764.1:p.Asn335=