Canonical Allele Identifier: CA1788938334
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63073000_63073003delinsGCCT , CM000670.2:g.63073000_63073003delinsGCCT GRCh38
NC_000008.10:g.63985559_63985562delinsGCCT , CM000670.1:g.63985559_63985562delinsGCCT GRCh37
NC_000008.9:g.64148113_64148116delinsGCCT NCBI36
NG_016123.1:g.18051_18054delinsAGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.290_293delinsAGGC MANE Select ENSP00000260116.4:p.Lys97=
ENST00000260116.4:c.290_293delinsAGGC ENSP00000260116.4:p.Lys97=
ENST00000521138.1:n.232+12815_232+12818delinsAGGC
NM_000370.3:c.290_293delinsAGGC MANE Select NP_000361.1:p.Lys97=
XM_006716468.2:c.205-8687_205-8684delinsAGGC XP_006716531.1:n.205-8687_205-8684delinsAGGC
XM_006716468.4:c.205-8687_205-8684delinsAGGC XP_006716531.1:n.205-8687_205-8684delinsAGGC