Canonical Allele Identifier: CA371333745
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072982A>C , CM000670.2:g.63072982A>C GRCh38
NC_000008.10:g.63985541A>C , CM000670.1:g.63985541A>C GRCh37
NC_000008.9:g.64148095A>C NCBI36
NG_016123.1:g.18072T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.311T>G MANE Select ENSP00000260116.4:p.Leu104Arg
ENST00000260116.4:c.311T>G ENSP00000260116.4:p.Leu104Arg
ENST00000521138.1:n.232+12836T>G
NM_000370.3:c.311T>G MANE Select NP_000361.1:p.Leu104Arg
XM_006716468.2:c.205-8666T>G XP_006716531.1:n.205-8666T>G
XM_006716468.4:c.205-8666T>G XP_006716531.1:n.205-8666T>G