Canonical Allele Identifier: CA379923713

Gene: ANO5

Linked Data

• COSMIC: COSM3986099
• MyVariant Identifiers: chr11:g.22294380C>A (hg19) ; chr11:g.22272834C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.97C>A
ENST00000682266.1:c.1630C>A	ENSP00000507766.1:p.Pro544Thr
ENST00000682341.1:c.2038C>A	ENSP00000508251.1:p.Pro680Thr
ENST00000683197.1:c.2038C>A	ENSP00000507641.1:p.Pro680Thr
ENST00000683411.1:c.1630C>A	ENSP00000508397.1:p.Pro544Thr
ENST00000683437.1:c.1630C>A	ENSP00000508408.1:p.Pro544Thr
ENST00000683613.1:n.3074C>A
ENST00000684663.1:c.2035C>A	ENSP00000508009.1:p.Pro679Thr
ENST00000324559.9:c.2080C>A MANE Select	ENSP00000315371.9:p.Pro694Thr
ENST00000648804.1:n.2415C>A
ENST00000324559.8:c.2080C>A	ENSP00000315371.8:p.Pro694Thr
ENST00000532043.1:n.97C>A
NM_001142649.1:c.2077C>A	NP_001136121.1:p.Pro693Thr
NM_213599.2:c.2080C>A , LRG_868t1:c.2080C>A	NP_998764.1:p.Pro694Thr
XM_005252820.2:c.2038C>A	XP_005252877.2:p.Pro680Thr
XM_005252821.2:c.2035C>A	XP_005252878.2:p.Pro679Thr
XM_005252822.3:c.2002C>A	XP_005252879.1:p.Pro668Thr
XM_005252823.3:c.1999C>A	XP_005252880.1:p.Pro667Thr
XM_011519949.1:c.1987C>A	XP_011518251.1:p.Pro663Thr
XM_005252820.3:c.2038C>A	XP_005252877.2:p.Pro680Thr
XM_005252821.3:c.2035C>A	XP_005252878.2:p.Pro679Thr
XM_005252822.4:c.2002C>A	XP_005252879.1:p.Pro668Thr
XM_011519949.2:c.1987C>A	XP_011518251.1:p.Pro663Thr
NM_001142649.2:c.2077C>A	NP_001136121.1:p.Pro693Thr
NM_213599.3:c.2080C>A MANE Select	NP_998764.1:p.Pro694Thr