Canonical Allele Identifier: CA1788938271
Gene: TTPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072857_63072861delinsAAGAG , CM000670.2:g.63072857_63072861delinsAAGAG GRCh38
NC_000008.10:g.63985416_63985420delinsAAGAG , CM000670.1:g.63985416_63985420delinsAAGAG GRCh37
NC_000008.9:g.64147970_64147974delinsAAGAG NCBI36
NG_016123.1:g.18193_18197delinsCTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.358+74_358+78delinsCTCTT MANE Select ENSP00000260116.4:n.358+74_358+78delinsCTCTT
ENST00000260116.4:c.358+74_358+78delinsCTCTT ENSP00000260116.4:n.358+74_358+78delinsCTCTT
ENST00000521138.1:n.232+12957_232+12961delinsCTCTT
NM_000370.3:c.358+74_358+78delinsCTCTT MANE Select NP_000361.1:n.358+74_358+78delinsCTCTT
XM_006716468.2:c.205-8545_205-8541delinsCTCTT XP_006716531.1:n.205-8545_205-8541delinsCTCTT
XM_006716468.4:c.205-8545_205-8541delinsCTCTT XP_006716531.1:n.205-8545_205-8541delinsCTCTT