Canonical Allele Identifier: CA379921427

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22276953C>A (hg19) ; chr11:g.22255407C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22255407C>A , CM000673.2:g.22255407C>A	GRCh38
NC_000011.9:g.22276953C>A , CM000673.1:g.22276953C>A	GRCh37
NC_000011.8:g.22233529C>A	NCBI36
NG_015844.1:g.67232C>A , LRG_868:g.67232C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682089.1:n.537C>A
ENST00000682266.1:c.767C>A	ENSP00000507766.1:p.Ala256Asp
ENST00000682341.1:c.1175C>A	ENSP00000508251.1:p.Ala392Asp
ENST00000682530.1:c.*1149C>A	ENSP00000506805.1:n.*1149C>A
ENST00000683197.1:c.1175C>A	ENSP00000507641.1:p.Ala392Asp
ENST00000683411.1:c.767C>A	ENSP00000508397.1:p.Ala256Asp
ENST00000683437.1:c.767C>A	ENSP00000508408.1:p.Ala256Asp
ENST00000683613.1:n.2211C>A
ENST00000683834.1:n.1417C>A
ENST00000684663.1:c.1172C>A	ENSP00000508009.1:p.Ala391Asp
ENST00000324559.9:c.1217C>A MANE Select	ENSP00000315371.9:p.Ala406Asp
ENST00000648804.1:n.1552C>A
ENST00000324559.8:c.1217C>A	ENSP00000315371.8:p.Ala406Asp
NM_001142649.1:c.1214C>A	NP_001136121.1:p.Ala405Asp
NM_213599.2:c.1217C>A , LRG_868t1:c.1217C>A	NP_998764.1:p.Ala406Asp
XM_005252820.2:c.1175C>A	XP_005252877.2:p.Ala392Asp
XM_005252821.2:c.1172C>A	XP_005252878.2:p.Ala391Asp
XM_005252822.3:c.1139C>A	XP_005252879.1:p.Ala380Asp
XM_005252823.3:c.1136C>A	XP_005252880.1:p.Ala379Asp
XM_011519949.1:c.1124C>A	XP_011518251.1:p.Ala375Asp
XM_005252820.3:c.1175C>A	XP_005252877.2:p.Ala392Asp
XM_005252821.3:c.1172C>A	XP_005252878.2:p.Ala391Asp
XM_005252822.4:c.1139C>A	XP_005252879.1:p.Ala380Asp
XM_011519949.2:c.1124C>A	XP_011518251.1:p.Ala375Asp
NM_001142649.2:c.1214C>A	NP_001136121.1:p.Ala405Asp
NM_213599.3:c.1217C>A MANE Select	NP_998764.1:p.Ala406Asp