Canonical Allele Identifier: CA10630646

Gene: ANO5

Linked Data

• ClinVar Variation Id: 304145
• ClinVar RCV Id: RCV000271617 ; RCV000328962 ; RCV001106814 ; RCV001786357
• dbSNP Id: rs142192440
• gnomAD v2: 11-22303406-G-A
• gnomAD v3: 11-22281860-G-A
• gnomAD v4: 11-22281860-G-A
• MyVariant Identifiers: chr11:g.22303406G>A (hg19) ; chr11:g.22281860G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22281860G>A , CM000673.2:g.22281860G>A	GRCh38
NC_000011.9:g.22303406G>A , CM000673.1:g.22303406G>A	GRCh37
NC_000011.8:g.22259982G>A	NCBI36
NG_015844.1:g.93685G>A , LRG_868:g.93685G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682266.1:c.*2095G>A	ENSP00000507766.1:n.*2095G>A
ENST00000682341.1:c.*2095G>A	ENSP00000508251.1:n.*2095G>A
ENST00000683197.1:c.*2301G>A	ENSP00000507641.1:n.*2301G>A
ENST00000683411.1:c.*2095G>A	ENSP00000508397.1:n.*2095G>A
ENST00000683437.1:c.*2095G>A	ENSP00000508408.1:n.*2095G>A
ENST00000683613.1:n.5831G>A
ENST00000684663.1:c.*2095G>A	ENSP00000508009.1:n.*2095G>A
ENST00000324559.9:c.*2095G>A MANE Select	ENSP00000315371.9:n.*2095G>A
ENST00000648804.1:n.5172G>A
ENST00000324559.8:c.*2095G>A	ENSP00000315371.8:n.*2095G>A
NM_001142649.1:c.*2095G>A	NP_001136121.1:n.*2095G>A
NM_213599.2:c.*2095G>A , LRG_868t1:c.*2095G>A	NP_998764.1:n.*2095G>A
XM_005252820.2:c.*2095G>A	XP_005252877.2:n.*2095G>A
XM_005252821.2:c.*2095G>A	XP_005252878.2:n.*2095G>A
XM_005252822.3:c.*2095G>A	XP_005252879.1:n.*2095G>A
XM_005252823.3:c.*2095G>A	XP_005252880.1:n.*2095G>A
XM_011519949.1:c.*2095G>A	XP_011518251.1:n.*2095G>A
XM_005252820.3:c.*2095G>A	XP_005252877.2:n.*2095G>A
XM_005252821.3:c.*2095G>A	XP_005252878.2:n.*2095G>A
XM_005252822.4:c.*2095G>A	XP_005252879.1:n.*2095G>A
XM_011519949.2:c.*2095G>A	XP_011518251.1:n.*2095G>A
NM_001142649.2:c.*2095G>A	NP_001136121.1:n.*2095G>A
NM_213599.3:c.*2095G>A MANE Select	NP_998764.1:n.*2095G>A