Canonical Allele Identifier: CA1788938296
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072906_63072908delinsGAA , CM000670.2:g.63072906_63072908delinsGAA GRCh38
NC_000008.10:g.63985465_63985467delinsGAA , CM000670.1:g.63985465_63985467delinsGAA GRCh37
NC_000008.9:g.64148019_64148021delinsGAA NCBI36
NG_016123.1:g.18146_18148delinsTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+27_358+29delinsTTC MANE Select ENSP00000260116.4:n.358+27_358+29delinsTT...
ENST00000260116.4:c.358+27_358+29delinsTTC ENSP00000260116.4:n.358+27_358+29delinsTT...
ENST00000521138.1:n.232+12910_232+12912delinsTTC
NM_000370.3:c.358+27_358+29delinsTTC MANE Select NP_000361.1:n.358+27_358+29delinsTTC
XM_006716468.2:c.205-8592_205-8590delinsTTC XP_006716531.1:n.205-8592_205-8590delinsT...
XM_006716468.4:c.205-8592_205-8590delinsTTC XP_006716531.1:n.205-8592_205-8590delinsT...