Canonical Allele Identifier: CA371333780
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072998C>A , CM000670.2:g.63072998C>A GRCh38
NC_000008.10:g.63985557C>A , CM000670.1:g.63985557C>A GRCh37
NC_000008.9:g.64148111C>A NCBI36
NG_016123.1:g.18056G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.295G>T MANE Select ENSP00000260116.4:p.Gly99Cys
ENST00000260116.4:c.295G>T ENSP00000260116.4:p.Gly99Cys
ENST00000521138.1:n.232+12820G>T
NM_000370.3:c.295G>T MANE Select NP_000361.1:p.Gly99Cys
XM_006716468.2:c.205-8682G>T XP_006716531.1:n.205-8682G>T
XM_006716468.4:c.205-8682G>T XP_006716531.1:n.205-8682G>T