Canonical Allele Identifier: CA2723540860

Gene: ANO5

Linked Data

• dbSNP Id: rs2133577687

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22218158C>T , CM000673.2:g.22218158C>T	GRCh38
NC_000011.9:g.22239704C>T , CM000673.1:g.22239704C>T	GRCh37
NC_000011.8:g.22196280C>T	NCBI36
NG_015844.1:g.29983C>T , LRG_868:g.29983C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682084.1:n.3313-88C>T
ENST00000682266.1:c.-270-2939C>T	ENSP00000507766.1:n.-270-2939C>T
ENST00000682341.1:c.139-2939C>T	ENSP00000508251.1:n.139-2939C>T
ENST00000682530.1:c.136-585C>T	ENSP00000506805.1:n.136-585C>T
ENST00000682684.1:n.560-2939C>T
ENST00000683197.1:c.139-2939C>T	ENSP00000507641.1:n.139-2939C>T
ENST00000683411.1:c.-270-2939C>T	ENSP00000508397.1:n.-270-2939C>T
ENST00000683437.1:c.-270-2939C>T	ENSP00000508408.1:n.-270-2939C>T
ENST00000683834.1:n.381-2939C>T
ENST00000683897.1:n.425-2939C>T
ENST00000684365.1:n.550-2939C>T
ENST00000684663.1:c.136-2939C>T	ENSP00000508009.1:n.136-2939C>T
ENST00000324559.9:c.139-88C>T MANE Select	ENSP00000315371.9:n.139-88C>T
ENST00000648804.1:n.670-428C>T
ENST00000324559.8:c.139-88C>T	ENSP00000315371.8:n.139-88C>T
NM_001142649.1:c.136-88C>T	NP_001136121.1:n.136-88C>T
NM_213599.2:c.139-88C>T , LRG_868t1:c.139-88C>T	NP_998764.1:n.139-88C>T
XM_005252820.2:c.139-2939C>T	XP_005252877.2:n.139-2939C>T
XM_005252821.2:c.136-2939C>T	XP_005252878.2:n.136-2939C>T
XM_005252822.3:c.61-88C>T	XP_005252879.1:n.61-88C>T
XM_005252823.3:c.58-88C>T	XP_005252880.1:n.58-88C>T
XM_011519949.1:c.88-2939C>T	XP_011518251.1:n.88-2939C>T
XM_005252820.3:c.139-2939C>T	XP_005252877.2:n.139-2939C>T
XM_005252821.3:c.136-2939C>T	XP_005252878.2:n.136-2939C>T
XM_005252822.4:c.61-88C>T	XP_005252879.1:n.61-88C>T
XM_011519949.2:c.88-2939C>T	XP_011518251.1:n.88-2939C>T
NM_001142649.2:c.136-88C>T	NP_001136121.1:n.136-88C>T
NM_213599.3:c.139-88C>T MANE Select	NP_998764.1:n.139-88C>T