Canonical Allele Identifier: CA1788938291
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072901G= , CM000670.2:g.63072901G= GRCh38
NC_000008.10:g.63985460G= , CM000670.1:g.63985460G= GRCh37
NC_000008.9:g.64148014G= NCBI36
NG_016123.1:g.18153C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+34C= MANE Select ENSP00000260116.4:n.358+34C=
ENST00000260116.4:c.358+34C= ENSP00000260116.4:n.358+34C=
ENST00000521138.1:n.232+12917C=
NM_000370.3:c.358+34C= MANE Select NP_000361.1:n.358+34C=
XM_006716468.2:c.205-8585C= XP_006716531.1:n.205-8585C=
XM_006716468.4:c.205-8585C= XP_006716531.1:n.205-8585C=