Canonical Allele Identifier: CA371333779
Gene: TTPA HGNC NCBI

Linked Data

gnomAD v4: 8-63072997-C-A

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.296G>T MANE Select ENSP00000260116.4:p.Gly99Val
ENST00000260116.4:c.296G>T ENSP00000260116.4:p.Gly99Val
ENST00000521138.1:n.232+12821G>T
NM_000370.3:c.296G>T MANE Select NP_000361.1:p.Gly99Val
XM_006716468.2:c.205-8681G>T XP_006716531.1:n.205-8681G>T
XM_006716468.4:c.205-8681G>T XP_006716531.1:n.205-8681G>T