Canonical Allele Identifier: CA473405088

Gene: ANO5

Linked Data

• gnomAD v4: 11-22259656-A-T
• MyVariant Identifiers: chr11:g.22281202A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259656A>T , CM000673.2:g.22259656A>T	GRCh38
NC_000011.9:g.22281202A>T , CM000673.1:g.22281202A>T	GRCh37
NC_000011.8:g.22237778A>T	NCBI36
NG_015844.1:g.71481A>T , LRG_868:g.71481A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1095A>T	ENSP00000507766.1:p.Ser365=
ENST00000682341.1:c.1503A>T	ENSP00000508251.1:p.Ser501=
ENST00000683197.1:c.1503A>T	ENSP00000507641.1:p.Ser501=
ENST00000683411.1:c.1095A>T	ENSP00000508397.1:p.Ser365=
ENST00000683437.1:c.1095A>T	ENSP00000508408.1:p.Ser365=
ENST00000683613.1:n.2539A>T
ENST00000684663.1:c.1500A>T	ENSP00000508009.1:p.Ser500=
ENST00000324559.9:c.1545A>T MANE Select	ENSP00000315371.9:p.Ser515=
ENST00000648804.1:n.1880A>T
ENST00000324559.8:c.1545A>T	ENSP00000315371.8:p.Ser515=
NM_001142649.1:c.1542A>T	NP_001136121.1:p.Ser514=
NM_213599.2:c.1545A>T , LRG_868t1:c.1545A>T	NP_998764.1:p.Ser515=
XM_005252820.2:c.1503A>T	XP_005252877.2:p.Ser501=
XM_005252821.2:c.1500A>T	XP_005252878.2:p.Ser500=
XM_005252822.3:c.1467A>T	XP_005252879.1:p.Ser489=
XM_005252823.3:c.1464A>T	XP_005252880.1:p.Ser488=
XM_011519949.1:c.1452A>T	XP_011518251.1:p.Ser484=
XM_005252820.3:c.1503A>T	XP_005252877.2:p.Ser501=
XM_005252821.3:c.1500A>T	XP_005252878.2:p.Ser500=
XM_005252822.4:c.1467A>T	XP_005252879.1:p.Ser489=
XM_011519949.2:c.1452A>T	XP_011518251.1:p.Ser484=
NM_001142649.2:c.1542A>T	NP_001136121.1:p.Ser514=
NM_213599.3:c.1545A>T MANE Select	NP_998764.1:p.Ser515=