Canonical Allele Identifier: CA1957419818

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262162G= , CM000673.2:g.22262162G=	GRCh38
NC_000011.9:g.22283708G= , CM000673.1:g.22283708G=	GRCh37
NC_000011.8:g.22240284G=	NCBI36
NG_015844.1:g.73987G= , LRG_868:g.73987G=

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1664G= MANE Select	NP_998764.1:p.Ser555=
ENST00000324559.9:c.1664G= MANE Select	ENSP00000315371.9:p.Ser555=
NM_001142649.1:c.1661G=	NP_001136121.1:p.Ser554=
NM_001142649.2:c.1661G=	NP_001136121.1:p.Ser554=
NM_213599.2:c.1664G= , LRG_868t1:c.1664G=	NP_998764.1:p.Ser555=
ENST00000324559.8:c.1664G=	ENSP00000315371.8:p.Ser555=
ENST00000648804.1:n.1999G=
ENST00000682266.1:c.1214G=	ENSP00000507766.1:p.Ser405=
ENST00000682341.1:c.1622G=	ENSP00000508251.1:p.Ser541=
ENST00000683197.1:c.1622G=	ENSP00000507641.1:p.Ser541=
ENST00000683411.1:c.1214G=	ENSP00000508397.1:p.Ser405=
ENST00000683437.1:c.1214G=	ENSP00000508408.1:p.Ser405=
ENST00000683613.1:n.2658G=
ENST00000684663.1:c.1619G=	ENSP00000508009.1:p.Ser540=
XM_005252820.2:c.1622G=	XP_005252877.2:p.Ser541=
XM_005252820.3:c.1622G=	XP_005252877.2:p.Ser541=
XM_005252821.2:c.1619G=	XP_005252878.2:p.Ser540=
XM_005252821.3:c.1619G=	XP_005252878.2:p.Ser540=
XM_005252822.3:c.1586G=	XP_005252879.1:p.Ser529=
XM_005252822.4:c.1586G=	XP_005252879.1:p.Ser529=
XM_005252823.3:c.1583G=	XP_005252880.1:p.Ser528=
XM_011519949.1:c.1571G=	XP_011518251.1:p.Ser524=
XM_011519949.2:c.1571G=	XP_011518251.1:p.Ser524=