Canonical Allele Identifier: CA13732131
Gene: ANKLE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132727588A>G , CM000674.2:g.132727588A>G GRCh38
NC_000012.11:g.133304174A>G , CM000674.1:g.133304174A>G GRCh37
NC_000012.10:g.131814247A>G NCBI36
NG_034022.1:g.39301T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000357997.10:c.2616-145T>C MANE Select ENSP00000350686.5:n.2616-145T>C
ENST00000357997.9:c.2616-145T>C ENSP00000350686.5:n.2616-145T>C
ENST00000538766.1:c.681-145T>C ENSP00000445760.1:n.681-145T>C
ENST00000539605.5:n.9115-145T>C
ENST00000542282.5:c.681-145T>C ENSP00000437807.1:n.681-145T>C
ENST00000542374.5:n.358-145T>C
ENST00000542657.5:c.681-145T>C ENSP00000438551.1:n.681-145T>C
NM_015114.2:c.2616-145T>C NP_055929.1:n.2616-145T>C
XM_005266159.2:c.2430-145T>C XP_005266216.1:n.2430-145T>C
XM_005266160.1:c.2430-145T>C XP_005266217.1:n.2430-145T>C
XM_006719735.1:c.2024-145T>C XP_006719798.1:n.2024-145T>C
XM_011534789.1:c.1305-145T>C XP_011533091.1:n.1305-145T>C
XM_005266159.3:c.2430-145T>C XP_005266216.1:n.2430-145T>C
XM_005266160.2:c.2430-145T>C XP_005266217.1:n.2430-145T>C
XM_024448899.1:c.1305-145T>C XP_024304667.1:n.1305-145T>C
XR_001748638.1:n.2538-145T>C
NM_015114.3:c.2616-145T>C MANE Select NP_055929.1:n.2616-145T>C