Canonical Allele Identifier: CA4763267
Gene: TTPA HGNC NCBI

Linked Data

dbSNP Id: rs760779083
ExAC: 8:63985465 G / GA
gnomAD v2: 8-63985465-G-GA
gnomAD v3: 8-63072906-G-GA
gnomAD v4: 8-63072906-G-GA
MyVariant Identifiers: chr8:g.63985466_63985467insA (hg19) chr8:g.63985465_63985466insA (hg19) chr8:g.63072907_63072908insA (hg38) chr8:g.63072906_63072907insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072916dup , CM000670.2:g.63072916dup GRCh38
NC_000008.10:g.63985475dup , CM000670.1:g.63985475dup GRCh37
NC_000008.9:g.64148029dup NCBI36
NG_016123.1:g.18147dup

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+28dup MANE Select ENSP00000260116.4:n.358+28dup
ENST00000260116.4:c.358+28dup ENSP00000260116.4:n.358+28dup
ENST00000521138.1:n.232+12911dup
NM_000370.3:c.358+28dup MANE Select NP_000361.1:n.358+28dup
XM_006716468.2:c.205-8591dup XP_006716531.1:n.205-8591dup
XM_006716468.4:c.205-8591dup XP_006716531.1:n.205-8591dup
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