Canonical Allele Identifier: CA2615728914

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798188A>G , CM000673.2:g.102798188A>G GRCh38
NC_000011.9:g.102668919A>G , CM000673.1:g.102668919A>G GRCh37
NC_000011.8:g.102174129A>G NCBI36
NG_011740.1:g.5048T>C
NG_011740.2:g.5048T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+66A>G (WTAPP1)
ENST00000525739.6:n.682+66A>G (WTAPP1)
ENST00000544704.1:n.443+66A>G (WTAPP1)
NM_001145938.1:c.-142T>C (MMP1) NP_001139410.1:n.-142T>C
NM_002421.3:c.-96T>C (MMP1) NP_002412.1:n.-96T>C
NR_038390.1:n.682+66A>G (WTAPP1)