Canonical Allele Identifier: CA10604433

Gene: ANO5

Linked Data

• ClinVar Variation Id: 283234
• ClinVar RCV Id: RCV001859575
• dbSNP Id: rs886042582
• MyVariant Identifiers: chr11:g.22294380C>T (hg19) ; chr11:g.22272834C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272834C>T , CM000673.2:g.22272834C>T	GRCh38
NC_000011.9:g.22294380C>T , CM000673.1:g.22294380C>T	GRCh37
NC_000011.8:g.22250956C>T	NCBI36
NG_015844.1:g.84659C>T , LRG_868:g.84659C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.97C>T
ENST00000682266.1:c.1630C>T	ENSP00000507766.1:p.Pro544Ser
ENST00000682341.1:c.2038C>T	ENSP00000508251.1:p.Pro680Ser
ENST00000683197.1:c.2038C>T	ENSP00000507641.1:p.Pro680Ser
ENST00000683411.1:c.1630C>T	ENSP00000508397.1:p.Pro544Ser
ENST00000683437.1:c.1630C>T	ENSP00000508408.1:p.Pro544Ser
ENST00000683613.1:n.3074C>T
ENST00000684663.1:c.2035C>T	ENSP00000508009.1:p.Pro679Ser
ENST00000324559.9:c.2080C>T MANE Select	ENSP00000315371.9:p.Pro694Ser
ENST00000648804.1:n.2415C>T
ENST00000324559.8:c.2080C>T	ENSP00000315371.8:p.Pro694Ser
ENST00000532043.1:n.97C>T
NM_001142649.1:c.2077C>T	NP_001136121.1:p.Pro693Ser
NM_213599.2:c.2080C>T , LRG_868t1:c.2080C>T	NP_998764.1:p.Pro694Ser
XM_005252820.2:c.2038C>T	XP_005252877.2:p.Pro680Ser
XM_005252821.2:c.2035C>T	XP_005252878.2:p.Pro679Ser
XM_005252822.3:c.2002C>T	XP_005252879.1:p.Pro668Ser
XM_005252823.3:c.1999C>T	XP_005252880.1:p.Pro667Ser
XM_011519949.1:c.1987C>T	XP_011518251.1:p.Pro663Ser
XM_005252820.3:c.2038C>T	XP_005252877.2:p.Pro680Ser
XM_005252821.3:c.2035C>T	XP_005252878.2:p.Pro679Ser
XM_005252822.4:c.2002C>T	XP_005252879.1:p.Pro668Ser
XM_011519949.2:c.1987C>T	XP_011518251.1:p.Pro663Ser
NM_001142649.2:c.2077C>T	NP_001136121.1:p.Pro693Ser
NM_213599.3:c.2080C>T MANE Select	NP_998764.1:p.Pro694Ser