Canonical Allele Identifier: CA2615728966

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798226_102798227insGA , CM000673.2:g.102798226_102798227insGA GRCh38
NC_000011.9:g.102668957_102668958insGA , CM000673.1:g.102668957_102668958insGA GRCh37
NC_000011.8:g.102174167_102174168insGA NCBI36
NG_011740.1:g.5009_5010insTC
NG_011740.2:g.5009_5010insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+104_423+105insGA (WTAPP1)
ENST00000525739.6:n.682+104_682+105insGA (WTAPP1)
ENST00000544704.1:n.443+104_443+105insGA (WTAPP1)
NM_001145938.1:c.-181_-180insTC (MMP1) NP_001139410.1:n.-181_-180insTC
NM_002421.3:c.-135_-134insTC (MMP1) NP_002412.1:n.-135_-134insTC
NR_038390.1:n.682+104_682+105insGA (WTAPP1)