Canonical Allele Identifier: CA379924049

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294528C>A (hg19) ; chr11:g.22272982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272982C>A , CM000673.2:g.22272982C>A	GRCh38
NC_000011.9:g.22294528C>A , CM000673.1:g.22294528C>A	GRCh37
NC_000011.8:g.22251104C>A	NCBI36
NG_015844.1:g.84807C>A , LRG_868:g.84807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532043.2:n.245C>A
ENST00000682266.1:c.1778C>A	ENSP00000507766.1:p.Ala593Glu
ENST00000682341.1:c.2186C>A	ENSP00000508251.1:p.Ala729Glu
ENST00000683197.1:c.2186C>A	ENSP00000507641.1:p.Ala729Glu
ENST00000683411.1:c.1778C>A	ENSP00000508397.1:p.Ala593Glu
ENST00000683437.1:c.1778C>A	ENSP00000508408.1:p.Ala593Glu
ENST00000683613.1:n.3222C>A
ENST00000684663.1:c.2183C>A	ENSP00000508009.1:p.Ala728Glu
ENST00000324559.9:c.2228C>A MANE Select	ENSP00000315371.9:p.Ala743Glu
ENST00000648804.1:n.2563C>A
ENST00000324559.8:c.2228C>A	ENSP00000315371.8:p.Ala743Glu
ENST00000532043.1:n.245C>A
NM_001142649.1:c.2225C>A	NP_001136121.1:p.Ala742Glu
NM_213599.2:c.2228C>A , LRG_868t1:c.2228C>A	NP_998764.1:p.Ala743Glu
XM_005252820.2:c.2186C>A	XP_005252877.2:p.Ala729Glu
XM_005252821.2:c.2183C>A	XP_005252878.2:p.Ala728Glu
XM_005252822.3:c.2150C>A	XP_005252879.1:p.Ala717Glu
XM_005252823.3:c.2147C>A	XP_005252880.1:p.Ala716Glu
XM_011519949.1:c.2135C>A	XP_011518251.1:p.Ala712Glu
XM_005252820.3:c.2186C>A	XP_005252877.2:p.Ala729Glu
XM_005252821.3:c.2183C>A	XP_005252878.2:p.Ala728Glu
XM_005252822.4:c.2150C>A	XP_005252879.1:p.Ala717Glu
XM_011519949.2:c.2135C>A	XP_011518251.1:p.Ala712Glu
NM_001142649.2:c.2225C>A	NP_001136121.1:p.Ala742Glu
NM_213599.3:c.2228C>A MANE Select	NP_998764.1:p.Ala743Glu