Canonical Allele Identifier: CA2580078853
Gene: TTPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2184158
ClinVar RCV Id: RCV002599978
gnomAD v4: 8-63072921-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072921T>C , CM000670.2:g.63072921T>C GRCh38
NC_000008.10:g.63985480T>C , CM000670.1:g.63985480T>C GRCh37
NC_000008.9:g.64148034T>C NCBI36
NG_016123.1:g.18133A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.358+14A>G MANE Select ENSP00000260116.4:n.358+14A>G
ENST00000260116.4:c.358+14A>G ENSP00000260116.4:n.358+14A>G
ENST00000521138.1:n.232+12897A>G
NM_000370.3:c.358+14A>G MANE Select NP_000361.1:n.358+14A>G
XM_006716468.2:c.205-8605A>G XP_006716531.1:n.205-8605A>G
XM_006716468.4:c.205-8605A>G XP_006716531.1:n.205-8605A>G