Canonical Allele Identifier: CA2615728969

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798228C>T , CM000673.2:g.102798228C>T GRCh38
NC_000011.9:g.102668959C>T , CM000673.1:g.102668959C>T GRCh37
NC_000011.8:g.102174169C>T NCBI36
NG_011740.1:g.5008G>A
NG_011740.2:g.5008G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+106C>T (WTAPP1)
ENST00000525739.6:n.682+106C>T (WTAPP1)
ENST00000544704.1:n.443+106C>T (WTAPP1)
NM_001145938.1:c.-182G>A (MMP1) NP_001139410.1:n.-182G>A
NM_002421.3:c.-136G>A (MMP1) NP_002412.1:n.-136G>A
NR_038390.1:n.682+106C>T (WTAPP1)