Canonical Allele Identifier: CA379923354

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22270373C>T , CM000673.2:g.22270373C>T	GRCh38
NC_000011.9:g.22291919C>T , CM000673.1:g.22291919C>T	GRCh37
NC_000011.8:g.22248495C>T	NCBI36
NG_015844.1:g.82198C>T , LRG_868:g.82198C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1960C>T MANE Select	NP_998764.1:p.Arg654Ter
ENST00000324559.9:c.1960C>T MANE Select	ENSP00000315371.9:p.Arg654Ter
NM_001142649.1:c.1957C>T	NP_001136121.1:p.Arg653Ter
NM_001142649.2:c.1957C>T	NP_001136121.1:p.Arg653Ter
NM_213599.2:c.1960C>T , LRG_868t1:c.1960C>T	NP_998764.1:p.Arg654Ter
ENST00000324559.8:c.1960C>T	ENSP00000315371.8:p.Arg654Ter
ENST00000648804.1:n.2295C>T
ENST00000682266.1:c.1510C>T	ENSP00000507766.1:p.Arg504Ter
ENST00000682341.1:c.1918C>T	ENSP00000508251.1:p.Arg640Ter
ENST00000683197.1:c.1918C>T	ENSP00000507641.1:p.Arg640Ter
ENST00000683411.1:c.1510C>T	ENSP00000508397.1:p.Arg504Ter
ENST00000683437.1:c.1510C>T	ENSP00000508408.1:p.Arg504Ter
ENST00000683613.1:n.2954C>T
ENST00000684663.1:c.1915C>T	ENSP00000508009.1:p.Arg639Ter
XM_005252820.2:c.1918C>T	XP_005252877.2:p.Arg640Ter
XM_005252820.3:c.1918C>T	XP_005252877.2:p.Arg640Ter
XM_005252821.2:c.1915C>T	XP_005252878.2:p.Arg639Ter
XM_005252821.3:c.1915C>T	XP_005252878.2:p.Arg639Ter
XM_005252822.3:c.1882C>T	XP_005252879.1:p.Arg628Ter
XM_005252822.4:c.1882C>T	XP_005252879.1:p.Arg628Ter
XM_005252823.3:c.1879C>T	XP_005252880.1:p.Arg627Ter
XM_011519949.1:c.1867C>T	XP_011518251.1:p.Arg623Ter
XM_011519949.2:c.1867C>T	XP_011518251.1:p.Arg623Ter