Canonical Allele Identifier: CA379920637

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22271785A>G (hg19) ; chr11:g.22250239A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22250239A>G , CM000673.2:g.22250239A>G	GRCh38
NC_000011.9:g.22271785A>G , CM000673.1:g.22271785A>G	GRCh37
NC_000011.8:g.22228361A>G	NCBI36
NG_015844.1:g.62064A>G , LRG_868:g.62064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682089.1:n.201A>G
ENST00000682266.1:c.431A>G	ENSP00000507766.1:p.Asn144Ser
ENST00000682341.1:c.839A>G	ENSP00000508251.1:p.Asn280Ser
ENST00000682530.1:c.*813A>G	ENSP00000506805.1:n.*813A>G
ENST00000683197.1:c.839A>G	ENSP00000507641.1:p.Asn280Ser
ENST00000683411.1:c.431A>G	ENSP00000508397.1:p.Asn144Ser
ENST00000683437.1:c.431A>G	ENSP00000508408.1:p.Asn144Ser
ENST00000683613.1:n.1875A>G
ENST00000683834.1:n.1081A>G
ENST00000684663.1:c.836A>G	ENSP00000508009.1:p.Asn279Ser
ENST00000324559.9:c.881A>G MANE Select	ENSP00000315371.9:p.Asn294Ser
ENST00000648804.1:n.1216A>G
ENST00000324559.8:c.881A>G	ENSP00000315371.8:p.Asn294Ser
NM_001142649.1:c.878A>G	NP_001136121.1:p.Asn293Ser
NM_213599.2:c.881A>G , LRG_868t1:c.881A>G	NP_998764.1:p.Asn294Ser
XM_005252820.2:c.839A>G	XP_005252877.2:p.Asn280Ser
XM_005252821.2:c.836A>G	XP_005252878.2:p.Asn279Ser
XM_005252822.3:c.803A>G	XP_005252879.1:p.Asn268Ser
XM_005252823.3:c.800A>G	XP_005252880.1:p.Asn267Ser
XM_011519949.1:c.788A>G	XP_011518251.1:p.Asn263Ser
XM_005252820.3:c.839A>G	XP_005252877.2:p.Asn280Ser
XM_005252821.3:c.836A>G	XP_005252878.2:p.Asn279Ser
XM_005252822.4:c.803A>G	XP_005252879.1:p.Asn268Ser
XM_011519949.2:c.788A>G	XP_011518251.1:p.Asn263Ser
NM_001142649.2:c.878A>G	NP_001136121.1:p.Asn293Ser
NM_213599.3:c.881A>G MANE Select	NP_998764.1:p.Asn294Ser