Canonical Allele Identifier: CA2574781333

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22225888A>T , CM000673.2:g.22225888A>T	GRCh38
NC_000011.9:g.22247434A>T , CM000673.1:g.22247434A>T	GRCh37
NC_000011.8:g.22204010A>T	NCBI36
NG_015844.1:g.37713A>T , LRG_868:g.37713A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.-156-96A>T	ENSP00000507766.1:n.-156-96A>T
ENST00000682341.1:c.253-96A>T	ENSP00000508251.1:n.253-96A>T
ENST00000682530.1:c.*227-96A>T	ENSP00000506805.1:n.*227-96A>T
ENST00000682684.1:n.674-96A>T
ENST00000683197.1:c.253-96A>T	ENSP00000507641.1:n.253-96A>T
ENST00000683411.1:c.-156-96A>T	ENSP00000508397.1:n.-156-96A>T
ENST00000683437.1:c.-156-96A>T	ENSP00000508408.1:n.-156-96A>T
ENST00000683613.1:n.1289-96A>T
ENST00000683834.1:n.495-96A>T
ENST00000684663.1:c.250-96A>T	ENSP00000508009.1:n.250-96A>T
ENST00000324559.9:c.295-96A>T MANE Select	ENSP00000315371.9:n.295-96A>T
ENST00000648804.1:n.860-96A>T
ENST00000324559.8:c.295-96A>T	ENSP00000315371.8:n.295-96A>T
NM_001142649.1:c.292-96A>T	NP_001136121.1:n.292-96A>T
NM_213599.2:c.295-96A>T , LRG_868t1:c.295-96A>T	NP_998764.1:n.295-96A>T
XM_005252820.2:c.253-96A>T	XP_005252877.2:n.253-96A>T
XM_005252821.2:c.250-96A>T	XP_005252878.2:n.250-96A>T
XM_005252822.3:c.217-96A>T	XP_005252879.1:n.217-96A>T
XM_005252823.3:c.214-96A>T	XP_005252880.1:n.214-96A>T
XM_011519949.1:c.202-96A>T	XP_011518251.1:n.202-96A>T
XM_005252820.3:c.253-96A>T	XP_005252877.2:n.253-96A>T
XM_005252821.3:c.250-96A>T	XP_005252878.2:n.250-96A>T
XM_005252822.4:c.217-96A>T	XP_005252879.1:n.217-96A>T
XM_011519949.2:c.202-96A>T	XP_011518251.1:n.202-96A>T
NM_001142649.2:c.292-96A>T	NP_001136121.1:n.292-96A>T
NM_213599.3:c.295-96A>T MANE Select	NP_998764.1:n.295-96A>T