Canonical Allele Identifier: CA2615728917

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798191_102798192insC , CM000673.2:g.102798191_102798192insC GRCh38
NC_000011.9:g.102668922_102668923insC , CM000673.1:g.102668922_102668923insC GRCh37
NC_000011.8:g.102174132_102174133insC NCBI36
NG_011740.1:g.5044_5045insG
NG_011740.2:g.5044_5045insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+69_423+70insC (WTAPP1)
ENST00000525739.6:n.682+69_682+70insC (WTAPP1)
ENST00000544704.1:n.443+69_443+70insC (WTAPP1)
NM_001145938.1:c.-146_-145insG (MMP1) NP_001139410.1:n.-146_-145insG
NM_002421.3:c.-100_-99insG (MMP1) NP_002412.1:n.-100_-99insG
NR_038390.1:n.682+69_682+70insC (WTAPP1)