Canonical Allele Identifier: CA371333758
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072988C>T , CM000670.2:g.63072988C>T GRCh38
NC_000008.10:g.63985547C>T , CM000670.1:g.63985547C>T GRCh37
NC_000008.9:g.64148101C>T NCBI36
NG_016123.1:g.18066G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.305G>A MANE Select ENSP00000260116.4:p.Gly102Glu
ENST00000260116.4:c.305G>A ENSP00000260116.4:p.Gly102Glu
ENST00000521138.1:n.232+12830G>A
NM_000370.3:c.305G>A MANE Select NP_000361.1:p.Gly102Glu
XM_006716468.2:c.205-8672G>A XP_006716531.1:n.205-8672G>A
XM_006716468.4:c.205-8672G>A XP_006716531.1:n.205-8672G>A