Canonical Allele Identifier: CA218743836

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22239354A>T , CM000673.2:g.22239354A>T	GRCh38
NC_000011.9:g.22260900A>T , CM000673.1:g.22260900A>T	GRCh37
NC_000011.8:g.22217476A>T	NCBI36
NG_015844.1:g.51179A>T , LRG_868:g.51179A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.763-215A>T MANE Select	NP_998764.1:n.763-215A>T
ENST00000324559.9:c.763-215A>T MANE Select	ENSP00000315371.9:n.763-215A>T
NM_001142649.1:c.760-215A>T	NP_001136121.1:n.760-215A>T
NM_001142649.2:c.760-215A>T	NP_001136121.1:n.760-215A>T
NM_213599.2:c.763-215A>T , LRG_868t1:c.763-215A>T	NP_998764.1:n.763-215A>T
ENST00000324559.8:c.763-215A>T	ENSP00000315371.8:n.763-215A>T
ENST00000648804.1:n.1214-10883A>T
ENST00000682266.1:c.313-215A>T	ENSP00000507766.1:n.313-215A>T
ENST00000682341.1:c.721-215A>T	ENSP00000508251.1:n.721-215A>T
ENST00000682530.1:c.*695-215A>T	ENSP00000506805.1:n.*695-215A>T
ENST00000682684.1:n.1142-215A>T
ENST00000683197.1:c.721-215A>T	ENSP00000507641.1:n.721-215A>T
ENST00000683411.1:c.313-215A>T	ENSP00000508397.1:n.313-215A>T
ENST00000683437.1:c.313-215A>T	ENSP00000508408.1:n.313-215A>T
ENST00000683613.1:n.1757-215A>T
ENST00000683834.1:n.963-215A>T
ENST00000684663.1:c.718-215A>T	ENSP00000508009.1:n.718-215A>T
XM_005252820.2:c.721-215A>T	XP_005252877.2:n.721-215A>T
XM_005252820.3:c.721-215A>T	XP_005252877.2:n.721-215A>T
XM_005252821.2:c.718-215A>T	XP_005252878.2:n.718-215A>T
XM_005252821.3:c.718-215A>T	XP_005252878.2:n.718-215A>T
XM_005252822.3:c.685-215A>T	XP_005252879.1:n.685-215A>T
XM_005252822.4:c.685-215A>T	XP_005252879.1:n.685-215A>T
XM_005252823.3:c.682-215A>T	XP_005252880.1:n.682-215A>T
XM_011519949.1:c.670-215A>T	XP_011518251.1:n.670-215A>T
XM_011519949.2:c.670-215A>T	XP_011518251.1:n.670-215A>T