Canonical Allele Identifier: CA2840057003

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259474G>T , CM000673.2:g.22259474G>T	GRCh38
NC_000011.9:g.22281020G>T , CM000673.1:g.22281020G>T	GRCh37
NC_000011.8:g.22237596G>T	NCBI36
NG_015844.1:g.71299G>T , LRG_868:g.71299G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.958-45G>T	ENSP00000507766.1:n.958-45G>T
ENST00000682341.1:c.1366-45G>T	ENSP00000508251.1:n.1366-45G>T
ENST00000683197.1:c.1366-45G>T	ENSP00000507641.1:n.1366-45G>T
ENST00000683411.1:c.958-45G>T	ENSP00000508397.1:n.958-45G>T
ENST00000683437.1:c.958-45G>T	ENSP00000508408.1:n.958-45G>T
ENST00000683613.1:n.2402-45G>T
ENST00000684663.1:c.1363-45G>T	ENSP00000508009.1:n.1363-45G>T
ENST00000324559.9:c.1408-45G>T MANE Select	ENSP00000315371.9:n.1408-45G>T
ENST00000648804.1:n.1743-45G>T
ENST00000324559.8:c.1408-45G>T	ENSP00000315371.8:n.1408-45G>T
NM_001142649.1:c.1405-45G>T	NP_001136121.1:n.1405-45G>T
NM_213599.2:c.1408-45G>T , LRG_868t1:c.1408-45G>T	NP_998764.1:n.1408-45G>T
XM_005252820.2:c.1366-45G>T	XP_005252877.2:n.1366-45G>T
XM_005252821.2:c.1363-45G>T	XP_005252878.2:n.1363-45G>T
XM_005252822.3:c.1330-45G>T	XP_005252879.1:n.1330-45G>T
XM_005252823.3:c.1327-45G>T	XP_005252880.1:n.1327-45G>T
XM_011519949.1:c.1315-45G>T	XP_011518251.1:n.1315-45G>T
XM_005252820.3:c.1366-45G>T	XP_005252877.2:n.1366-45G>T
XM_005252821.3:c.1363-45G>T	XP_005252878.2:n.1363-45G>T
XM_005252822.4:c.1330-45G>T	XP_005252879.1:n.1330-45G>T
XM_011519949.2:c.1315-45G>T	XP_011518251.1:n.1315-45G>T
NM_001142649.2:c.1405-45G>T	NP_001136121.1:n.1405-45G>T
NM_213599.3:c.1408-45G>T MANE Select	NP_998764.1:n.1408-45G>T