Canonical Allele Identifier: CA371333765
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072991T>A , CM000670.2:g.63072991T>A GRCh38
NC_000008.10:g.63985550T>A , CM000670.1:g.63985550T>A GRCh37
NC_000008.9:g.64148104T>A NCBI36
NG_016123.1:g.18063A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.302A>T MANE Select ENSP00000260116.4:p.His101Leu
ENST00000260116.4:c.302A>T ENSP00000260116.4:p.His101Leu
ENST00000521138.1:n.232+12827A>T
NM_000370.3:c.302A>T MANE Select NP_000361.1:p.His101Leu
XM_006716468.2:c.205-8675A>T XP_006716531.1:n.205-8675A>T
XM_006716468.4:c.205-8675A>T XP_006716531.1:n.205-8675A>T