Canonical Allele Identifier: CA379922524

Gene: ANO5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22262154T>G , CM000673.2:g.22262154T>G	GRCh38
NC_000011.9:g.22283700T>G , CM000673.1:g.22283700T>G	GRCh37
NC_000011.8:g.22240276T>G	NCBI36
NG_015844.1:g.73979T>G , LRG_868:g.73979T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_213599.3:c.1656T>G MANE Select	NP_998764.1:p.Tyr552Ter
ENST00000324559.9:c.1656T>G MANE Select	ENSP00000315371.9:p.Tyr552Ter
NM_001142649.1:c.1653T>G	NP_001136121.1:p.Tyr551Ter
NM_001142649.2:c.1653T>G	NP_001136121.1:p.Tyr551Ter
NM_213599.2:c.1656T>G , LRG_868t1:c.1656T>G	NP_998764.1:p.Tyr552Ter
ENST00000324559.8:c.1656T>G	ENSP00000315371.8:p.Tyr552Ter
ENST00000648804.1:n.1991T>G
ENST00000682266.1:c.1206T>G	ENSP00000507766.1:p.Tyr402Ter
ENST00000682341.1:c.1614T>G	ENSP00000508251.1:p.Tyr538Ter
ENST00000683197.1:c.1614T>G	ENSP00000507641.1:p.Tyr538Ter
ENST00000683411.1:c.1206T>G	ENSP00000508397.1:p.Tyr402Ter
ENST00000683437.1:c.1206T>G	ENSP00000508408.1:p.Tyr402Ter
ENST00000683613.1:n.2650T>G
ENST00000684663.1:c.1611T>G	ENSP00000508009.1:p.Tyr537Ter
XM_005252820.2:c.1614T>G	XP_005252877.2:p.Tyr538Ter
XM_005252820.3:c.1614T>G	XP_005252877.2:p.Tyr538Ter
XM_005252821.2:c.1611T>G	XP_005252878.2:p.Tyr537Ter
XM_005252821.3:c.1611T>G	XP_005252878.2:p.Tyr537Ter
XM_005252822.3:c.1578T>G	XP_005252879.1:p.Tyr526Ter
XM_005252822.4:c.1578T>G	XP_005252879.1:p.Tyr526Ter
XM_005252823.3:c.1575T>G	XP_005252880.1:p.Tyr525Ter
XM_011519949.1:c.1563T>G	XP_011518251.1:p.Tyr521Ter
XM_011519949.2:c.1563T>G	XP_011518251.1:p.Tyr521Ter