Canonical Allele Identifier: CA1788938311
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072938T= , CM000670.2:g.63072938T= GRCh38
NC_000008.10:g.63985497T= , CM000670.1:g.63985497T= GRCh37
NC_000008.9:g.64148051T= NCBI36
NG_016123.1:g.18116A=

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.355A= MANE Select ENSP00000260116.4:p.Ile119=
ENST00000260116.4:c.355A= ENSP00000260116.4:p.Ile119=
ENST00000521138.1:n.232+12880A=
NM_000370.3:c.355A= MANE Select NP_000361.1:p.Ile119=
XM_006716468.2:c.205-8622A= XP_006716531.1:n.205-8622A=
XM_006716468.4:c.205-8622A= XP_006716531.1:n.205-8622A=