Canonical Allele Identifier: CA6895890
Community Standard Title: NM_015114.3(ANKLE2):c.706C>T (p.Arg236Ter)
Gene: ANKLE2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.132750784G>A , CM000674.2:g.132750784G>A GRCh38
NC_000012.11:g.133327370G>A , CM000674.1:g.133327370G>A GRCh37
NC_000012.10:g.131837443G>A NCBI36
NG_034022.1:g.16105C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015114.3:c.706C>T MANE Select NP_055929.1:p.Arg236Ter
ENST00000357997.10:c.706C>T MANE Select ENSP00000350686.5:p.Arg236Ter
NM_015114.2:c.706C>T NP_055929.1:p.Arg236Ter
ENST00000357997.9:c.706C>T ENSP00000350686.5:p.Arg236Ter
ENST00000539605.5:n.7205C>T
ENST00000545623.5:n.551C>T
XM_005266159.2:c.520C>T XP_005266216.1:p.Arg174Ter
XM_005266159.3:c.520C>T XP_005266216.1:p.Arg174Ter
XM_005266160.1:c.520C>T XP_005266217.1:p.Arg174Ter
XM_005266160.2:c.520C>T XP_005266217.1:p.Arg174Ter
XM_005266161.1:c.706C>T XP_005266218.1:p.Arg236Ter
XM_006719735.1:c.706C>T XP_006719798.1:p.Arg236Ter
XM_011534787.1:c.706C>T XP_011533089.1:p.Arg236Ter
XM_011534787.3:c.706C>T XP_011533089.1:p.Arg236Ter
XM_011534788.1:c.706C>T XP_011533090.1:p.Arg236Ter
XM_024448899.1:c.-689C>T XP_024304667.1:n.-689C>T
XR_001748638.1:n.707C>T