Canonical Allele Identifier: CA5923225

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22257706C>G , CM000673.2:g.22257706C>G	GRCh38
NC_000011.9:g.22279252C>G , CM000673.1:g.22279252C>G	GRCh37
NC_000011.8:g.22235828C>G	NCBI36
NG_015844.1:g.69531C>G , LRG_868:g.69531C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1359C>G MANE Select	NP_998764.1:p.Tyr453Ter
ENST00000324559.9:c.1359C>G MANE Select	ENSP00000315371.9:p.Tyr453Ter
NM_001142649.1:c.1356C>G	NP_001136121.1:p.Tyr452Ter
NM_001142649.2:c.1356C>G	NP_001136121.1:p.Tyr452Ter
NM_213599.2:c.1359C>G , LRG_868t1:c.1359C>G	NP_998764.1:p.Tyr453Ter
ENST00000324559.8:c.1359C>G	ENSP00000315371.8:p.Tyr453Ter
ENST00000648804.1:n.1694C>G
ENST00000682266.1:c.909C>G	ENSP00000507766.1:p.Tyr303Ter
ENST00000682341.1:c.1317C>G	ENSP00000508251.1:p.Tyr439Ter
ENST00000683197.1:c.1317C>G	ENSP00000507641.1:p.Tyr439Ter
ENST00000683411.1:c.909C>G	ENSP00000508397.1:p.Tyr303Ter
ENST00000683437.1:c.909C>G	ENSP00000508408.1:p.Tyr303Ter
ENST00000683613.1:n.2353C>G
ENST00000684663.1:c.1314C>G	ENSP00000508009.1:p.Tyr438Ter
XM_005252820.2:c.1317C>G	XP_005252877.2:p.Tyr439Ter
XM_005252820.3:c.1317C>G	XP_005252877.2:p.Tyr439Ter
XM_005252821.2:c.1314C>G	XP_005252878.2:p.Tyr438Ter
XM_005252821.3:c.1314C>G	XP_005252878.2:p.Tyr438Ter
XM_005252822.3:c.1281C>G	XP_005252879.1:p.Tyr427Ter
XM_005252822.4:c.1281C>G	XP_005252879.1:p.Tyr427Ter
XM_005252823.3:c.1278C>G	XP_005252880.1:p.Tyr426Ter
XM_011519949.1:c.1266C>G	XP_011518251.1:p.Tyr422Ter
XM_011519949.2:c.1266C>G	XP_011518251.1:p.Tyr422Ter