Canonical Allele Identifier: CA1788938313
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072942G= , CM000670.2:g.63072942G= GRCh38
NC_000008.10:g.63985501G= , CM000670.1:g.63985501G= GRCh37
NC_000008.9:g.64148055G= NCBI36
NG_016123.1:g.18112C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.351C= MANE Select ENSP00000260116.4:p.Tyr117=
ENST00000260116.4:c.351C= ENSP00000260116.4:p.Tyr117=
ENST00000521138.1:n.232+12876C=
NM_000370.3:c.351C= MANE Select NP_000361.1:p.Tyr117=
XM_006716468.2:c.205-8626C= XP_006716531.1:n.205-8626C=
XM_006716468.4:c.205-8626C= XP_006716531.1:n.205-8626C=