Canonical Allele Identifier: CA1788938305
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072921T= , CM000670.2:g.63072921T= GRCh38
NC_000008.10:g.63985480T= , CM000670.1:g.63985480T= GRCh37
NC_000008.9:g.64148034T= NCBI36
NG_016123.1:g.18133A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.358+14A= MANE Select ENSP00000260116.4:n.358+14A=
ENST00000260116.4:c.358+14A= ENSP00000260116.4:n.358+14A=
ENST00000521138.1:n.232+12897A=
NM_000370.3:c.358+14A= MANE Select NP_000361.1:n.358+14A=
XM_006716468.2:c.205-8605A= XP_006716531.1:n.205-8605A=
XM_006716468.4:c.205-8605A= XP_006716531.1:n.205-8605A=