Canonical Allele Identifier: CA2687441782
Gene: TTPA HGNC NCBI

Linked Data

gnomAD v4: 8-63072926-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072926A>T , CM000670.2:g.63072926A>T GRCh38
NC_000008.10:g.63985485A>T , CM000670.1:g.63985485A>T GRCh37
NC_000008.9:g.64148039A>T NCBI36
NG_016123.1:g.18128T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+9T>A MANE Select ENSP00000260116.4:n.358+9T>A
ENST00000260116.4:c.358+9T>A ENSP00000260116.4:n.358+9T>A
ENST00000521138.1:n.232+12892T>A
NM_000370.3:c.358+9T>A MANE Select NP_000361.1:n.358+9T>A
XM_006716468.2:c.205-8610T>A XP_006716531.1:n.205-8610T>A
XM_006716468.4:c.205-8610T>A XP_006716531.1:n.205-8610T>A
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