Canonical Allele Identifier: CA379923988

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294498T>G (hg19) ; chr11:g.22272952T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272952T>G , CM000673.2:g.22272952T>G	GRCh38
NC_000011.9:g.22294498T>G , CM000673.1:g.22294498T>G	GRCh37
NC_000011.8:g.22251074T>G	NCBI36
NG_015844.1:g.84777T>G , LRG_868:g.84777T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.215T>G
ENST00000682266.1:c.1748T>G	ENSP00000507766.1:p.Ile583Ser
ENST00000682341.1:c.2156T>G	ENSP00000508251.1:p.Ile719Ser
ENST00000683197.1:c.2156T>G	ENSP00000507641.1:p.Ile719Ser
ENST00000683411.1:c.1748T>G	ENSP00000508397.1:p.Ile583Ser
ENST00000683437.1:c.1748T>G	ENSP00000508408.1:p.Ile583Ser
ENST00000683613.1:n.3192T>G
ENST00000684663.1:c.2153T>G	ENSP00000508009.1:p.Ile718Ser
ENST00000324559.9:c.2198T>G MANE Select	ENSP00000315371.9:p.Ile733Ser
ENST00000648804.1:n.2533T>G
ENST00000324559.8:c.2198T>G	ENSP00000315371.8:p.Ile733Ser
ENST00000532043.1:n.215T>G
NM_001142649.1:c.2195T>G	NP_001136121.1:p.Ile732Ser
NM_213599.2:c.2198T>G , LRG_868t1:c.2198T>G	NP_998764.1:p.Ile733Ser
XM_005252820.2:c.2156T>G	XP_005252877.2:p.Ile719Ser
XM_005252821.2:c.2153T>G	XP_005252878.2:p.Ile718Ser
XM_005252822.3:c.2120T>G	XP_005252879.1:p.Ile707Ser
XM_005252823.3:c.2117T>G	XP_005252880.1:p.Ile706Ser
XM_011519949.1:c.2105T>G	XP_011518251.1:p.Ile702Ser
XM_005252820.3:c.2156T>G	XP_005252877.2:p.Ile719Ser
XM_005252821.3:c.2153T>G	XP_005252878.2:p.Ile718Ser
XM_005252822.4:c.2120T>G	XP_005252879.1:p.Ile707Ser
XM_011519949.2:c.2105T>G	XP_011518251.1:p.Ile702Ser
NM_001142649.2:c.2195T>G	NP_001136121.1:p.Ile732Ser
NM_213599.3:c.2198T>G MANE Select	NP_998764.1:p.Ile733Ser