Canonical Allele Identifier: CA379923984

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294497A>G (hg19) ; chr11:g.22272951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272951A>G , CM000673.2:g.22272951A>G	GRCh38
NC_000011.9:g.22294497A>G , CM000673.1:g.22294497A>G	GRCh37
NC_000011.8:g.22251073A>G	NCBI36
NG_015844.1:g.84776A>G , LRG_868:g.84776A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.214A>G
ENST00000682266.1:c.1747A>G	ENSP00000507766.1:p.Ile583Val
ENST00000682341.1:c.2155A>G	ENSP00000508251.1:p.Ile719Val
ENST00000683197.1:c.2155A>G	ENSP00000507641.1:p.Ile719Val
ENST00000683411.1:c.1747A>G	ENSP00000508397.1:p.Ile583Val
ENST00000683437.1:c.1747A>G	ENSP00000508408.1:p.Ile583Val
ENST00000683613.1:n.3191A>G
ENST00000684663.1:c.2152A>G	ENSP00000508009.1:p.Ile718Val
ENST00000324559.9:c.2197A>G MANE Select	ENSP00000315371.9:p.Ile733Val
ENST00000648804.1:n.2532A>G
ENST00000324559.8:c.2197A>G	ENSP00000315371.8:p.Ile733Val
ENST00000532043.1:n.214A>G
NM_001142649.1:c.2194A>G	NP_001136121.1:p.Ile732Val
NM_213599.2:c.2197A>G , LRG_868t1:c.2197A>G	NP_998764.1:p.Ile733Val
XM_005252820.2:c.2155A>G	XP_005252877.2:p.Ile719Val
XM_005252821.2:c.2152A>G	XP_005252878.2:p.Ile718Val
XM_005252822.3:c.2119A>G	XP_005252879.1:p.Ile707Val
XM_005252823.3:c.2116A>G	XP_005252880.1:p.Ile706Val
XM_011519949.1:c.2104A>G	XP_011518251.1:p.Ile702Val
XM_005252820.3:c.2155A>G	XP_005252877.2:p.Ile719Val
XM_005252821.3:c.2152A>G	XP_005252878.2:p.Ile718Val
XM_005252822.4:c.2119A>G	XP_005252879.1:p.Ile707Val
XM_011519949.2:c.2104A>G	XP_011518251.1:p.Ile702Val
NM_001142649.2:c.2194A>G	NP_001136121.1:p.Ile732Val
NM_213599.3:c.2197A>G MANE Select	NP_998764.1:p.Ile733Val