Canonical Allele Identifier: CA379922323

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22281231T>A (hg19) ; chr11:g.22259685T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22259685T>A , CM000673.2:g.22259685T>A	GRCh38
NC_000011.9:g.22281231T>A , CM000673.1:g.22281231T>A	GRCh37
NC_000011.8:g.22237807T>A	NCBI36
NG_015844.1:g.71510T>A , LRG_868:g.71510T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.1124T>A	ENSP00000507766.1:p.Val375Asp
ENST00000682341.1:c.1532T>A	ENSP00000508251.1:p.Val511Asp
ENST00000683197.1:c.1532T>A	ENSP00000507641.1:p.Val511Asp
ENST00000683411.1:c.1124T>A	ENSP00000508397.1:p.Val375Asp
ENST00000683437.1:c.1124T>A	ENSP00000508408.1:p.Val375Asp
ENST00000683613.1:n.2568T>A
ENST00000684663.1:c.1529T>A	ENSP00000508009.1:p.Val510Asp
ENST00000324559.9:c.1574T>A MANE Select	ENSP00000315371.9:p.Val525Asp
ENST00000648804.1:n.1909T>A
ENST00000324559.8:c.1574T>A	ENSP00000315371.8:p.Val525Asp
NM_001142649.1:c.1571T>A	NP_001136121.1:p.Val524Asp
NM_213599.2:c.1574T>A , LRG_868t1:c.1574T>A	NP_998764.1:p.Val525Asp
XM_005252820.2:c.1532T>A	XP_005252877.2:p.Val511Asp
XM_005252821.2:c.1529T>A	XP_005252878.2:p.Val510Asp
XM_005252822.3:c.1496T>A	XP_005252879.1:p.Val499Asp
XM_005252823.3:c.1493T>A	XP_005252880.1:p.Val498Asp
XM_011519949.1:c.1481T>A	XP_011518251.1:p.Val494Asp
XM_005252820.3:c.1532T>A	XP_005252877.2:p.Val511Asp
XM_005252821.3:c.1529T>A	XP_005252878.2:p.Val510Asp
XM_005252822.4:c.1496T>A	XP_005252879.1:p.Val499Asp
XM_011519949.2:c.1481T>A	XP_011518251.1:p.Val494Asp
NM_001142649.2:c.1571T>A	NP_001136121.1:p.Val524Asp
NM_213599.3:c.1574T>A MANE Select	NP_998764.1:p.Val525Asp