Canonical Allele Identifier: CA379923980

Gene: ANO5

Linked Data

• MyVariant Identifiers: chr11:g.22294495A>T (hg19) ; chr11:g.22272949A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22272949A>T , CM000673.2:g.22272949A>T	GRCh38
NC_000011.9:g.22294495A>T , CM000673.1:g.22294495A>T	GRCh37
NC_000011.8:g.22251071A>T	NCBI36
NG_015844.1:g.84774A>T , LRG_868:g.84774A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000532043.2:n.212A>T
ENST00000682266.1:c.1745A>T	ENSP00000507766.1:p.Asp582Val
ENST00000682341.1:c.2153A>T	ENSP00000508251.1:p.Asp718Val
ENST00000683197.1:c.2153A>T	ENSP00000507641.1:p.Asp718Val
ENST00000683411.1:c.1745A>T	ENSP00000508397.1:p.Asp582Val
ENST00000683437.1:c.1745A>T	ENSP00000508408.1:p.Asp582Val
ENST00000683613.1:n.3189A>T
ENST00000684663.1:c.2150A>T	ENSP00000508009.1:p.Asp717Val
ENST00000324559.9:c.2195A>T MANE Select	ENSP00000315371.9:p.Asp732Val
ENST00000648804.1:n.2530A>T
ENST00000324559.8:c.2195A>T	ENSP00000315371.8:p.Asp732Val
ENST00000532043.1:n.212A>T
NM_001142649.1:c.2192A>T	NP_001136121.1:p.Asp731Val
NM_213599.2:c.2195A>T , LRG_868t1:c.2195A>T	NP_998764.1:p.Asp732Val
XM_005252820.2:c.2153A>T	XP_005252877.2:p.Asp718Val
XM_005252821.2:c.2150A>T	XP_005252878.2:p.Asp717Val
XM_005252822.3:c.2117A>T	XP_005252879.1:p.Asp706Val
XM_005252823.3:c.2114A>T	XP_005252880.1:p.Asp705Val
XM_011519949.1:c.2102A>T	XP_011518251.1:p.Asp701Val
XM_005252820.3:c.2153A>T	XP_005252877.2:p.Asp718Val
XM_005252821.3:c.2150A>T	XP_005252878.2:p.Asp717Val
XM_005252822.4:c.2117A>T	XP_005252879.1:p.Asp706Val
XM_011519949.2:c.2102A>T	XP_011518251.1:p.Asp701Val
NM_001142649.2:c.2192A>T	NP_001136121.1:p.Asp731Val
NM_213599.3:c.2195A>T MANE Select	NP_998764.1:p.Asp732Val