Canonical Allele Identifier: CA379923736

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294387T>G (hg19) ; chr11:g.22272841T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272841T>G , CM000673.2:g.22272841T>G	GRCh38
NC_000011.9:g.22294387T>G , CM000673.1:g.22294387T>G	GRCh37
NC_000011.8:g.22250963T>G	NCBI36
NG_015844.1:g.84666T>G , LRG_868:g.84666T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.104T>G
ENST00000682266.1:c.1637T>G	ENSP00000507766.1:p.Leu546Arg
ENST00000682341.1:c.2045T>G	ENSP00000508251.1:p.Leu682Arg
ENST00000683197.1:c.2045T>G	ENSP00000507641.1:p.Leu682Arg
ENST00000683411.1:c.1637T>G	ENSP00000508397.1:p.Leu546Arg
ENST00000683437.1:c.1637T>G	ENSP00000508408.1:p.Leu546Arg
ENST00000683613.1:n.3081T>G
ENST00000684663.1:c.2042T>G	ENSP00000508009.1:p.Leu681Arg
ENST00000324559.9:c.2087T>G MANE Select	ENSP00000315371.9:p.Leu696Arg
ENST00000648804.1:n.2422T>G
ENST00000324559.8:c.2087T>G	ENSP00000315371.8:p.Leu696Arg
ENST00000532043.1:n.104T>G
NM_001142649.1:c.2084T>G	NP_001136121.1:p.Leu695Arg
NM_213599.2:c.2087T>G , LRG_868t1:c.2087T>G	NP_998764.1:p.Leu696Arg
XM_005252820.2:c.2045T>G	XP_005252877.2:p.Leu682Arg
XM_005252821.2:c.2042T>G	XP_005252878.2:p.Leu681Arg
XM_005252822.3:c.2009T>G	XP_005252879.1:p.Leu670Arg
XM_005252823.3:c.2006T>G	XP_005252880.1:p.Leu669Arg
XM_011519949.1:c.1994T>G	XP_011518251.1:p.Leu665Arg
XM_005252820.3:c.2045T>G	XP_005252877.2:p.Leu682Arg
XM_005252821.3:c.2042T>G	XP_005252878.2:p.Leu681Arg
XM_005252822.4:c.2009T>G	XP_005252879.1:p.Leu670Arg
XM_011519949.2:c.1994T>G	XP_011518251.1:p.Leu665Arg
NM_001142649.2:c.2084T>G	NP_001136121.1:p.Leu695Arg
NM_213599.3:c.2087T>G MANE Select	NP_998764.1:p.Leu696Arg