Canonical Allele Identifier: CA371333776
Gene: TTPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.63985554A>T (hg19) chr8:g.63072995A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072995A>T , CM000670.2:g.63072995A>T GRCh38
NC_000008.10:g.63985554A>T , CM000670.1:g.63985554A>T GRCh37
NC_000008.9:g.64148108A>T NCBI36
NG_016123.1:g.18059T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.298T>A MANE Select ENSP00000260116.4:p.Tyr100Asn
ENST00000260116.4:c.298T>A ENSP00000260116.4:p.Tyr100Asn
ENST00000521138.1:n.232+12823T>A
NM_000370.3:c.298T>A MANE Select NP_000361.1:p.Tyr100Asn
XM_006716468.2:c.205-8679T>A XP_006716531.1:n.205-8679T>A
XM_006716468.4:c.205-8679T>A XP_006716531.1:n.205-8679T>A
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