Canonical Allele Identifier: CA2615728947

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798218G>T , CM000673.2:g.102798218G>T GRCh38
NC_000011.9:g.102668949G>T , CM000673.1:g.102668949G>T GRCh37
NC_000011.8:g.102174159G>T NCBI36
NG_011740.1:g.5018C>A
NG_011740.2:g.5018C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+96G>T (WTAPP1)
ENST00000525739.6:n.682+96G>T (WTAPP1)
ENST00000544704.1:n.443+96G>T (WTAPP1)
NM_001145938.1:c.-172C>A (MMP1) NP_001139410.1:n.-172C>A
NM_002421.3:c.-126C>A (MMP1) NP_002412.1:n.-126C>A
NR_038390.1:n.682+96G>T (WTAPP1)