Canonical Allele Identifier: CA1957402770

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272827T= , CM000673.2:g.22272827T=	GRCh38
NC_000011.9:g.22294373T= , CM000673.1:g.22294373T=	GRCh37
NC_000011.8:g.22250949T=	NCBI36
NG_015844.1:g.84652T= , LRG_868:g.84652T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.90T=
ENST00000682266.1:c.1623T=	ENSP00000507766.1:p.Pro541=
ENST00000682341.1:c.2031T=	ENSP00000508251.1:p.Pro677=
ENST00000683197.1:c.2031T=	ENSP00000507641.1:p.Pro677=
ENST00000683411.1:c.1623T=	ENSP00000508397.1:p.Pro541=
ENST00000683437.1:c.1623T=	ENSP00000508408.1:p.Pro541=
ENST00000683613.1:n.3067T=
ENST00000684663.1:c.2028T=	ENSP00000508009.1:p.Pro676=
ENST00000324559.9:c.2073T= MANE Select	ENSP00000315371.9:p.Pro691=
ENST00000648804.1:n.2408T=
ENST00000324559.8:c.2073T=	ENSP00000315371.8:p.Pro691=
ENST00000532043.1:n.90T=
NM_001142649.1:c.2070T=	NP_001136121.1:p.Pro690=
NM_213599.2:c.2073T= , LRG_868t1:c.2073T=	NP_998764.1:p.Pro691=
XM_005252820.2:c.2031T=	XP_005252877.2:p.Pro677=
XM_005252821.2:c.2028T=	XP_005252878.2:p.Pro676=
XM_005252822.3:c.1995T=	XP_005252879.1:p.Pro665=
XM_005252823.3:c.1992T=	XP_005252880.1:p.Pro664=
XM_011519949.1:c.1980T=	XP_011518251.1:p.Pro660=
XM_005252820.3:c.2031T=	XP_005252877.2:p.Pro677=
XM_005252821.3:c.2028T=	XP_005252878.2:p.Pro676=
XM_005252822.4:c.1995T=	XP_005252879.1:p.Pro665=
XM_011519949.2:c.1980T=	XP_011518251.1:p.Pro660=
NM_001142649.2:c.2070T=	NP_001136121.1:p.Pro690=
NM_213599.3:c.2073T= MANE Select	NP_998764.1:p.Pro691=