Canonical Allele Identifier: CA5922948

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22227508A>G , CM000673.2:g.22227508A>G	GRCh38
NC_000011.9:g.22249054A>G , CM000673.1:g.22249054A>G	GRCh37
NC_000011.8:g.22205630A>G	NCBI36
NG_015844.1:g.39333A>G , LRG_868:g.39333A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.570A>G MANE Select	NP_998764.1:p.Gln190=
ENST00000324559.9:c.570A>G MANE Select	ENSP00000315371.9:p.Gln190=
NM_001142649.1:c.567A>G	NP_001136121.1:p.Gln189=
NM_001142649.2:c.567A>G	NP_001136121.1:p.Gln189=
NM_213599.2:c.570A>G , LRG_868t1:c.570A>G	NP_998764.1:p.Gln190=
ENST00000324559.8:c.570A>G	ENSP00000315371.8:p.Gln190=
ENST00000648804.1:n.1135A>G
ENST00000682266.1:c.120A>G	ENSP00000507766.1:p.Gln40=
ENST00000682341.1:c.528A>G	ENSP00000508251.1:p.Gln176=
ENST00000682530.1:c.*502A>G	ENSP00000506805.1:n.*502A>G
ENST00000682684.1:n.949A>G
ENST00000683197.1:c.528A>G	ENSP00000507641.1:p.Gln176=
ENST00000683411.1:c.120A>G	ENSP00000508397.1:p.Gln40=
ENST00000683437.1:c.120A>G	ENSP00000508408.1:p.Gln40=
ENST00000683613.1:n.1564A>G
ENST00000683834.1:n.770A>G
ENST00000684663.1:c.525A>G	ENSP00000508009.1:p.Gln175=
XM_005252820.2:c.528A>G	XP_005252877.2:p.Gln176=
XM_005252820.3:c.528A>G	XP_005252877.2:p.Gln176=
XM_005252821.2:c.525A>G	XP_005252878.2:p.Gln175=
XM_005252821.3:c.525A>G	XP_005252878.2:p.Gln175=
XM_005252822.3:c.492A>G	XP_005252879.1:p.Gln164=
XM_005252822.4:c.492A>G	XP_005252879.1:p.Gln164=
XM_005252823.3:c.489A>G	XP_005252880.1:p.Gln163=
XM_011519949.1:c.477A>G	XP_011518251.1:p.Gln159=
XM_011519949.2:c.477A>G	XP_011518251.1:p.Gln159=