Canonical Allele Identifier: CA379922950

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22284528C>T (hg19) ; chr11:g.22262982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262982C>T , CM000673.2:g.22262982C>T	GRCh38
NC_000011.9:g.22284528C>T , CM000673.1:g.22284528C>T	GRCh37
NC_000011.8:g.22241104C>T	NCBI36
NG_015844.1:g.74807C>T , LRG_868:g.74807C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682266.1:c.1387C>T	ENSP00000507766.1:p.Gln463Ter
ENST00000682341.1:c.1795C>T	ENSP00000508251.1:p.Gln599Ter
ENST00000683197.1:c.1795C>T	ENSP00000507641.1:p.Gln599Ter
ENST00000683411.1:c.1387C>T	ENSP00000508397.1:p.Gln463Ter
ENST00000683437.1:c.1387C>T	ENSP00000508408.1:p.Gln463Ter
ENST00000683613.1:n.2831C>T
ENST00000684663.1:c.1792C>T	ENSP00000508009.1:p.Gln598Ter
ENST00000324559.9:c.1837C>T MANE Select	ENSP00000315371.9:p.Gln613Ter
ENST00000648804.1:n.2172C>T
ENST00000324559.8:c.1837C>T	ENSP00000315371.8:p.Gln613Ter
NM_001142649.1:c.1834C>T	NP_001136121.1:p.Gln612Ter
NM_213599.2:c.1837C>T , LRG_868t1:c.1837C>T	NP_998764.1:p.Gln613Ter
XM_005252820.2:c.1795C>T	XP_005252877.2:p.Gln599Ter
XM_005252821.2:c.1792C>T	XP_005252878.2:p.Gln598Ter
XM_005252822.3:c.1759C>T	XP_005252879.1:p.Gln587Ter
XM_005252823.3:c.1756C>T	XP_005252880.1:p.Gln586Ter
XM_011519949.1:c.1744C>T	XP_011518251.1:p.Gln582Ter
XM_005252820.3:c.1795C>T	XP_005252877.2:p.Gln599Ter
XM_005252821.3:c.1792C>T	XP_005252878.2:p.Gln598Ter
XM_005252822.4:c.1759C>T	XP_005252879.1:p.Gln587Ter
XM_011519949.2:c.1744C>T	XP_011518251.1:p.Gln582Ter
NM_001142649.2:c.1834C>T	NP_001136121.1:p.Gln612Ter
NM_213599.3:c.1837C>T MANE Select	NP_998764.1:p.Gln613Ter