Canonical Allele Identifier: CA5922845

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22221174C>A , CM000673.2:g.22221174C>A	GRCh38
NC_000011.9:g.22242720C>A , CM000673.1:g.22242720C>A	GRCh37
NC_000011.8:g.22199296C>A	NCBI36
NG_015844.1:g.32999C>A , LRG_868:g.32999C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.258C>A MANE Select	NP_998764.1:p.Tyr86Ter
ENST00000324559.9:c.258C>A MANE Select	ENSP00000315371.9:p.Tyr86Ter
NM_001142649.1:c.255C>A	NP_001136121.1:p.Tyr85Ter
NM_001142649.2:c.255C>A	NP_001136121.1:p.Tyr85Ter
NM_213599.2:c.258C>A , LRG_868t1:c.258C>A	NP_998764.1:p.Tyr86Ter
ENST00000324559.8:c.258C>A	ENSP00000315371.8:p.Tyr86Ter
ENST00000648804.1:n.823C>A
ENST00000682266.1:c.-193C>A	ENSP00000507766.1:n.-193C>A
ENST00000682341.1:c.216C>A	ENSP00000508251.1:p.Tyr72Ter
ENST00000682530.1:c.*190C>A	ENSP00000506805.1:n.*190C>A
ENST00000682684.1:n.637C>A
ENST00000683197.1:c.216C>A	ENSP00000507641.1:p.Tyr72Ter
ENST00000683411.1:c.-193C>A	ENSP00000508397.1:n.-193C>A
ENST00000683437.1:c.-193C>A	ENSP00000508408.1:n.-193C>A
ENST00000683613.1:n.1252C>A
ENST00000683834.1:n.458C>A
ENST00000683897.1:n.502C>A
ENST00000684365.1:n.627C>A
ENST00000684663.1:c.213C>A	ENSP00000508009.1:p.Tyr71Ter
XM_005252820.2:c.216C>A	XP_005252877.2:p.Tyr72Ter
XM_005252820.3:c.216C>A	XP_005252877.2:p.Tyr72Ter
XM_005252821.2:c.213C>A	XP_005252878.2:p.Tyr71Ter
XM_005252821.3:c.213C>A	XP_005252878.2:p.Tyr71Ter
XM_005252822.3:c.180C>A	XP_005252879.1:p.Tyr60Ter
XM_005252822.4:c.180C>A	XP_005252879.1:p.Tyr60Ter
XM_005252823.3:c.177C>A	XP_005252880.1:p.Tyr59Ter
XM_011519949.1:c.165C>A	XP_011518251.1:p.Tyr55Ter
XM_011519949.2:c.165C>A	XP_011518251.1:p.Tyr55Ter