Canonical Allele Identifier: CA1788938297
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072906G= , CM000670.2:g.63072906G= GRCh38
NC_000008.10:g.63985465G= , CM000670.1:g.63985465G= GRCh37
NC_000008.9:g.64148019G= NCBI36
NG_016123.1:g.18148C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+29C= MANE Select ENSP00000260116.4:n.358+29C=
ENST00000260116.4:c.358+29C= ENSP00000260116.4:n.358+29C=
ENST00000521138.1:n.232+12912C=
NM_000370.3:c.358+29C= MANE Select NP_000361.1:n.358+29C=
XM_006716468.2:c.205-8590C= XP_006716531.1:n.205-8590C=
XM_006716468.4:c.205-8590C= XP_006716531.1:n.205-8590C=