Canonical Allele Identifier: CA2410905760
Gene: NCAPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50523551_50523555delinsTCACA , CM000684.2:g.50523551_50523555delinsTCACA GRCh38
NC_000022.10:g.50961980_50961984delinsTCACA , CM000684.1:g.50961980_50961984delinsTCACA GRCh37
NC_000022.9:g.49308846_49308850delinsTCACA NCBI36
NG_016235.1:g.7885_7889delinsTGTGA
NG_021419.1:g.20336_20340delinsTCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000420993.7:c.*176_*180delinsTCACA MANE Select ENSP00000410088.2:n.*176_*180delinsTCACA
NM_001185011.1:c.*176_*180delinsTCACA NP_001171940.1:n.*176_*180delinsTCACA
NM_152299.3:c.*176_*180delinsTCACA NP_689512.2:n.*176_*180delinsTCACA
XR_001755232.1:n.2204_2208delinsTCACA
NM_152299.4:c.*176_*180delinsTCACA MANE Select NP_689512.2:n.*176_*180delinsTCACA
NM_001185011.2:c.*176_*180delinsTCACA NP_001171940.1:n.*176_*180delinsTCACA