Canonical Allele Identifier: CA1788938283
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072885C= , CM000670.2:g.63072885C= GRCh38
NC_000008.10:g.63985444C= , CM000670.1:g.63985444C= GRCh37
NC_000008.9:g.64147998C= NCBI36
NG_016123.1:g.18169G=

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+50G= MANE Select ENSP00000260116.4:n.358+50G=
ENST00000260116.4:c.358+50G= ENSP00000260116.4:n.358+50G=
ENST00000521138.1:n.232+12933G=
NM_000370.3:c.358+50G= MANE Select NP_000361.1:n.358+50G=
XM_006716468.2:c.205-8569G= XP_006716531.1:n.205-8569G=
XM_006716468.4:c.205-8569G= XP_006716531.1:n.205-8569G=