Canonical Allele Identifier: CA371333777
Gene: TTPA HGNC NCBI

Linked Data

gnomAD v4: 8-63072997-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072997C>T , CM000670.2:g.63072997C>T GRCh38
NC_000008.10:g.63985556C>T , CM000670.1:g.63985556C>T GRCh37
NC_000008.9:g.64148110C>T NCBI36
NG_016123.1:g.18057G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.296G>A MANE Select ENSP00000260116.4:p.Gly99Asp
ENST00000260116.4:c.296G>A ENSP00000260116.4:p.Gly99Asp
ENST00000521138.1:n.232+12821G>A
NM_000370.3:c.296G>A MANE Select NP_000361.1:p.Gly99Asp
XM_006716468.2:c.205-8681G>A XP_006716531.1:n.205-8681G>A
XM_006716468.4:c.205-8681G>A XP_006716531.1:n.205-8681G>A