Canonical Allele Identifier: CA1788938307
Gene: TTPA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072928G= , CM000670.2:g.63072928G= GRCh38
NC_000008.10:g.63985487G= , CM000670.1:g.63985487G= GRCh37
NC_000008.9:g.64148041G= NCBI36
NG_016123.1:g.18126C=

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+7C= MANE Select ENSP00000260116.4:n.358+7C=
ENST00000260116.4:c.358+7C= ENSP00000260116.4:n.358+7C=
ENST00000521138.1:n.232+12890C=
NM_000370.3:c.358+7C= MANE Select NP_000361.1:n.358+7C=
XM_006716468.2:c.205-8612C= XP_006716531.1:n.205-8612C=
XM_006716468.4:c.205-8612C= XP_006716531.1:n.205-8612C=
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