Canonical Allele Identifier: CA1957413200

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250298C= , CM000673.2:g.22250298C=	GRCh38
NC_000011.9:g.22271844C= , CM000673.1:g.22271844C=	GRCh37
NC_000011.8:g.22228420C=	NCBI36
NG_015844.1:g.62123C= , LRG_868:g.62123C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.260C=
ENST00000682266.1:c.490C=	ENSP00000507766.1:p.Leu164=
ENST00000682341.1:c.898C=	ENSP00000508251.1:p.Leu300=
ENST00000682530.1:c.*872C=	ENSP00000506805.1:n.*872C=
ENST00000683197.1:c.898C=	ENSP00000507641.1:p.Leu300=
ENST00000683411.1:c.490C=	ENSP00000508397.1:p.Leu164=
ENST00000683437.1:c.490C=	ENSP00000508408.1:p.Leu164=
ENST00000683613.1:n.1934C=
ENST00000683834.1:n.1140C=
ENST00000684663.1:c.895C=	ENSP00000508009.1:p.Leu299=
ENST00000324559.9:c.940C= MANE Select	ENSP00000315371.9:p.Leu314=
ENST00000648804.1:n.1275C=
ENST00000324559.8:c.940C=	ENSP00000315371.8:p.Leu314=
NM_001142649.1:c.937C=	NP_001136121.1:p.Leu313=
NM_213599.2:c.940C= , LRG_868t1:c.940C=	NP_998764.1:p.Leu314=
XM_005252820.2:c.898C=	XP_005252877.2:p.Leu300=
XM_005252821.2:c.895C=	XP_005252878.2:p.Leu299=
XM_005252822.3:c.862C=	XP_005252879.1:p.Leu288=
XM_005252823.3:c.859C=	XP_005252880.1:p.Leu287=
XM_011519949.1:c.847C=	XP_011518251.1:p.Leu283=
XM_005252820.3:c.898C=	XP_005252877.2:p.Leu300=
XM_005252821.3:c.895C=	XP_005252878.2:p.Leu299=
XM_005252822.4:c.862C=	XP_005252879.1:p.Leu288=
XM_011519949.2:c.847C=	XP_011518251.1:p.Leu283=
NM_001142649.2:c.937C=	NP_001136121.1:p.Leu313=
NM_213599.3:c.940C= MANE Select	NP_998764.1:p.Leu314=