Canonical Allele Identifier: CA2542052534
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072900_63072901insT , CM000670.2:g.63072900_63072901insT GRCh38
NC_000008.10:g.63985459_63985460insT , CM000670.1:g.63985459_63985460insT GRCh37
NC_000008.9:g.64148013_64148014insT NCBI36
NG_016123.1:g.18153_18154insA

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+34_358+35insA MANE Select ENSP00000260116.4:n.358+34_358+35insA
ENST00000260116.4:c.358+34_358+35insA ENSP00000260116.4:n.358+34_358+35insA
ENST00000521138.1:n.232+12917_232+12918insA
NM_000370.3:c.358+34_358+35insA MANE Select NP_000361.1:n.358+34_358+35insA
XM_006716468.2:c.205-8585_205-8584insA XP_006716531.1:n.205-8585_205-8584insA
XM_006716468.4:c.205-8585_205-8584insA XP_006716531.1:n.205-8585_205-8584insA