Canonical Allele Identifier: CA371333759
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072989C>A , CM000670.2:g.63072989C>A GRCh38
NC_000008.10:g.63985548C>A , CM000670.1:g.63985548C>A GRCh37
NC_000008.9:g.64148102C>A NCBI36
NG_016123.1:g.18065G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.304G>T MANE Select ENSP00000260116.4:p.Gly102Ter
ENST00000260116.4:c.304G>T ENSP00000260116.4:p.Gly102Ter
ENST00000521138.1:n.232+12829G>T
NM_000370.3:c.304G>T MANE Select NP_000361.1:p.Gly102Ter
XM_006716468.2:c.205-8673G>T XP_006716531.1:n.205-8673G>T
XM_006716468.4:c.205-8673G>T XP_006716531.1:n.205-8673G>T