Canonical Allele Identifier: CA601245913

Linked Data

dbSNP Id: rs1246698049

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789689del , CM000673.2:g.102789689del GRCh38
NC_000011.9:g.102660420del , CM000673.1:g.102660420del GRCh37
NC_000011.8:g.102165630del NCBI36
NG_011740.1:g.13550del
NG_011740.2:g.13550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1314del (MMP1)
ENST00000681445.1:n.1310del (MMP1)
ENST00000681643.1:n.1336del (MMP1)
ENST00000371455.7:n.325-8335del (WTAPP1)
ENST00000525739.6:n.390-3456del (WTAPP1)
ENST00000544704.1:n.344+5625del (WTAPP1)
NR_038390.1:n.390-3456del (WTAPP1)