Canonical Allele Identifier: CA473407324
Gene: ANO5 HGNC NCBI

Linked Data

dbSNP Id: rs1590306705
MyVariant Identifiers: chr11:g.22284521G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22262975G>A , CM000673.2:g.22262975G>A GRCh38
NC_000011.9:g.22284521G>A , CM000673.1:g.22284521G>A GRCh37
NC_000011.8:g.22241097G>A NCBI36
NG_015844.1:g.74800G>A , LRG_868:g.74800G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682266.1:c.1380G>A ENSP00000507766.1:p.Leu460=
ENST00000682341.1:c.1788G>A ENSP00000508251.1:p.Leu596=
ENST00000683197.1:c.1788G>A ENSP00000507641.1:p.Leu596=
ENST00000683411.1:c.1380G>A ENSP00000508397.1:p.Leu460=
ENST00000683437.1:c.1380G>A ENSP00000508408.1:p.Leu460=
ENST00000683613.1:n.2824G>A
ENST00000684663.1:c.1785G>A ENSP00000508009.1:p.Leu595=
ENST00000324559.9:c.1830G>A MANE Select ENSP00000315371.9:p.Leu610=
ENST00000648804.1:n.2165G>A
ENST00000324559.8:c.1830G>A ENSP00000315371.8:p.Leu610=
NM_001142649.1:c.1827G>A NP_001136121.1:p.Leu609=
NM_213599.2:c.1830G>A , LRG_868t1:c.1830G>A NP_998764.1:p.Leu610=
XM_005252820.2:c.1788G>A XP_005252877.2:p.Leu596=
XM_005252821.2:c.1785G>A XP_005252878.2:p.Leu595=
XM_005252822.3:c.1752G>A XP_005252879.1:p.Leu584=
XM_005252823.3:c.1749G>A XP_005252880.1:p.Leu583=
XM_011519949.1:c.1737G>A XP_011518251.1:p.Leu579=
XM_005252820.3:c.1788G>A XP_005252877.2:p.Leu596=
XM_005252821.3:c.1785G>A XP_005252878.2:p.Leu595=
XM_005252822.4:c.1752G>A XP_005252879.1:p.Leu584=
XM_011519949.2:c.1737G>A XP_011518251.1:p.Leu579=
NM_001142649.2:c.1827G>A NP_001136121.1:p.Leu609=
NM_213599.3:c.1830G>A MANE Select NP_998764.1:p.Leu610=