Canonical Allele Identifier: CA218752934
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs867275134

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22250348A>G , CM000673.2:g.22250348A>G GRCh38
NC_000011.9:g.22271894A>G , CM000673.1:g.22271894A>G GRCh37
NC_000011.8:g.22228470A>G NCBI36
NG_015844.1:g.62173A>G , LRG_868:g.62173A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682089.1:n.310A>G
ENST00000682266.1:c.540A>G ENSP00000507766.1:p.Leu180=
ENST00000682341.1:c.948A>G ENSP00000508251.1:p.Leu316=
ENST00000682530.1:c.*922A>G ENSP00000506805.1:n.*922A>G
ENST00000683197.1:c.948A>G ENSP00000507641.1:p.Leu316=
ENST00000683411.1:c.540A>G ENSP00000508397.1:p.Leu180=
ENST00000683437.1:c.540A>G ENSP00000508408.1:p.Leu180=
ENST00000683613.1:n.1984A>G
ENST00000683834.1:n.1190A>G
ENST00000684663.1:c.945A>G ENSP00000508009.1:p.Leu315=
ENST00000324559.9:c.990A>G MANE Select ENSP00000315371.9:p.Leu330=
ENST00000648804.1:n.1325A>G
ENST00000324559.8:c.990A>G ENSP00000315371.8:p.Leu330=
NM_001142649.1:c.987A>G NP_001136121.1:p.Leu329=
NM_213599.2:c.990A>G , LRG_868t1:c.990A>G NP_998764.1:p.Leu330=
XM_005252820.2:c.948A>G XP_005252877.2:p.Leu316=
XM_005252821.2:c.945A>G XP_005252878.2:p.Leu315=
XM_005252822.3:c.912A>G XP_005252879.1:p.Leu304=
XM_005252823.3:c.909A>G XP_005252880.1:p.Leu303=
XM_011519949.1:c.897A>G XP_011518251.1:p.Leu299=
XM_005252820.3:c.948A>G XP_005252877.2:p.Leu316=
XM_005252821.3:c.945A>G XP_005252878.2:p.Leu315=
XM_005252822.4:c.912A>G XP_005252879.1:p.Leu304=
XM_011519949.2:c.897A>G XP_011518251.1:p.Leu299=
NM_001142649.2:c.987A>G NP_001136121.1:p.Leu329=
NM_213599.3:c.990A>G MANE Select NP_998764.1:p.Leu330=