Canonical Allele Identifier: CA461144458
Gene: TTPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.63985495G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072936G>T , CM000670.2:g.63072936G>T GRCh38
NC_000008.10:g.63985495G>T , CM000670.1:g.63985495G>T GRCh37
NC_000008.9:g.64148049G>T NCBI36
NG_016123.1:g.18118C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.357C>A MANE Select ENSP00000260116.4:p.Ile119=
ENST00000260116.4:c.357C>A ENSP00000260116.4:p.Ile119=
ENST00000521138.1:n.232+12882C>A
NM_000370.3:c.357C>A MANE Select NP_000361.1:p.Ile119=
XM_006716468.2:c.205-8620C>A XP_006716531.1:n.205-8620C>A
XM_006716468.4:c.205-8620C>A XP_006716531.1:n.205-8620C>A
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