Canonical Allele Identifier: CA1957397330
Gene: ANO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22225768_22225770delinsTGG , CM000673.2:g.22225768_22225770delinsTGG GRCh38
NC_000011.9:g.22247314_22247316delinsTGG , CM000673.1:g.22247314_22247316delinsTGG GRCh37
NC_000011.8:g.22203890_22203892delinsTGG NCBI36
NG_015844.1:g.37593_37595delinsTGG , LRG_868:g.37593_37595delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682266.1:c.-156-216_-156-214delinsTGG ENSP00000507766.1:n.-156-216_-156-214delinsTGG
ENST00000682341.1:c.253-216_253-214delinsTGG ENSP00000508251.1:n.253-216_253-214delinsTGG
ENST00000682530.1:c.*227-216_*227-214delinsTGG ENSP00000506805.1:n.*227-216_*227-214delinsTGG
ENST00000682684.1:n.674-216_674-214delinsTGG
ENST00000683197.1:c.253-216_253-214delinsTGG ENSP00000507641.1:n.253-216_253-214delinsTGG
ENST00000683411.1:c.-156-216_-156-214delinsTGG ENSP00000508397.1:n.-156-216_-156-214delinsTGG
ENST00000683437.1:c.-156-216_-156-214delinsTGG ENSP00000508408.1:n.-156-216_-156-214delinsTGG
ENST00000683613.1:n.1289-216_1289-214delinsTGG
ENST00000683834.1:n.495-216_495-214delinsTGG
ENST00000684663.1:c.250-216_250-214delinsTGG ENSP00000508009.1:n.250-216_250-214delinsTGG
ENST00000324559.9:c.295-216_295-214delinsTGG MANE Select ENSP00000315371.9:n.295-216_295-214delinsTGG
ENST00000648804.1:n.860-216_860-214delinsTGG
ENST00000324559.8:c.295-216_295-214delinsTGG ENSP00000315371.8:n.295-216_295-214delinsTGG
NM_001142649.1:c.292-216_292-214delinsTGG NP_001136121.1:n.292-216_292-214delinsTGG
NM_213599.2:c.295-216_295-214delinsTGG , LRG_868t1:c.295-216_295-214delinsTGG NP_998764.1:n.295-216_295-214delinsTGG
XM_005252820.2:c.253-216_253-214delinsTGG XP_005252877.2:n.253-216_253-214delinsTGG
XM_005252821.2:c.250-216_250-214delinsTGG XP_005252878.2:n.250-216_250-214delinsTGG
XM_005252822.3:c.217-216_217-214delinsTGG XP_005252879.1:n.217-216_217-214delinsTGG
XM_005252823.3:c.214-216_214-214delinsTGG XP_005252880.1:n.214-216_214-214delinsTGG
XM_011519949.1:c.202-216_202-214delinsTGG XP_011518251.1:n.202-216_202-214delinsTGG
XM_005252820.3:c.253-216_253-214delinsTGG XP_005252877.2:n.253-216_253-214delinsTGG
XM_005252821.3:c.250-216_250-214delinsTGG XP_005252878.2:n.250-216_250-214delinsTGG
XM_005252822.4:c.217-216_217-214delinsTGG XP_005252879.1:n.217-216_217-214delinsTGG
XM_011519949.2:c.202-216_202-214delinsTGG XP_011518251.1:n.202-216_202-214delinsTGG
NM_001142649.2:c.292-216_292-214delinsTGG NP_001136121.1:n.292-216_292-214delinsTGG
NM_213599.3:c.295-216_295-214delinsTGG MANE Select NP_998764.1:n.295-216_295-214delinsTGG