Canonical Allele Identifier: CA2780587715
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072865_63072894dup , CM000670.2:g.63072865_63072894dup GRCh38
NC_000008.10:g.63985424_63985453dup , CM000670.1:g.63985424_63985453dup GRCh37
NC_000008.9:g.64147978_64148007dup NCBI36
NG_016123.1:g.18160_18189dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.358+41_358+70dup MANE Select ENSP00000260116.4:n.358+41_358+70dup
ENST00000260116.4:c.358+41_358+70dup ENSP00000260116.4:n.358+41_358+70dup
ENST00000521138.1:n.232+12924_232+12953dup
NM_000370.3:c.358+41_358+70dup MANE Select NP_000361.1:n.358+41_358+70dup
XM_006716468.2:c.205-8578_205-8549dup XP_006716531.1:n.205-8578_205-8549dup
XM_006716468.4:c.205-8578_205-8549dup XP_006716531.1:n.205-8578_205-8549dup