Canonical Allele Identifier: CA379922886

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22284498C>A (hg19) ; chr11:g.22262952C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262952C>A , CM000673.2:g.22262952C>A	GRCh38
NC_000011.9:g.22284498C>A , CM000673.1:g.22284498C>A	GRCh37
NC_000011.8:g.22241074C>A	NCBI36
NG_015844.1:g.74777C>A , LRG_868:g.74777C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1357C>A	ENSP00000507766.1:p.Pro453Thr
ENST00000682341.1:c.1765C>A	ENSP00000508251.1:p.Pro589Thr
ENST00000683197.1:c.1765C>A	ENSP00000507641.1:p.Pro589Thr
ENST00000683411.1:c.1357C>A	ENSP00000508397.1:p.Pro453Thr
ENST00000683437.1:c.1357C>A	ENSP00000508408.1:p.Pro453Thr
ENST00000683613.1:n.2801C>A
ENST00000684663.1:c.1762C>A	ENSP00000508009.1:p.Pro588Thr
ENST00000324559.9:c.1807C>A MANE Select	ENSP00000315371.9:p.Pro603Thr
ENST00000648804.1:n.2142C>A
ENST00000324559.8:c.1807C>A	ENSP00000315371.8:p.Pro603Thr
NM_001142649.1:c.1804C>A	NP_001136121.1:p.Pro602Thr
NM_213599.2:c.1807C>A , LRG_868t1:c.1807C>A	NP_998764.1:p.Pro603Thr
XM_005252820.2:c.1765C>A	XP_005252877.2:p.Pro589Thr
XM_005252821.2:c.1762C>A	XP_005252878.2:p.Pro588Thr
XM_005252822.3:c.1729C>A	XP_005252879.1:p.Pro577Thr
XM_005252823.3:c.1726C>A	XP_005252880.1:p.Pro576Thr
XM_011519949.1:c.1714C>A	XP_011518251.1:p.Pro572Thr
XM_005252820.3:c.1765C>A	XP_005252877.2:p.Pro589Thr
XM_005252821.3:c.1762C>A	XP_005252878.2:p.Pro588Thr
XM_005252822.4:c.1729C>A	XP_005252879.1:p.Pro577Thr
XM_011519949.2:c.1714C>A	XP_011518251.1:p.Pro572Thr
NM_001142649.2:c.1804C>A	NP_001136121.1:p.Pro602Thr
NM_213599.3:c.1807C>A MANE Select	NP_998764.1:p.Pro603Thr