Canonical Allele Identifier: CA371333771
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072994T>A , CM000670.2:g.63072994T>A GRCh38
NC_000008.10:g.63985553T>A , CM000670.1:g.63985553T>A GRCh37
NC_000008.9:g.64148107T>A NCBI36
NG_016123.1:g.18060A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.299A>T MANE Select ENSP00000260116.4:p.Tyr100Phe
ENST00000260116.4:c.299A>T ENSP00000260116.4:p.Tyr100Phe
ENST00000521138.1:n.232+12824A>T
NM_000370.3:c.299A>T MANE Select NP_000361.1:p.Tyr100Phe
XM_006716468.2:c.205-8678A>T XP_006716531.1:n.205-8678A>T
XM_006716468.4:c.205-8678A>T XP_006716531.1:n.205-8678A>T