Canonical Allele Identifier: CA2615724342

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789807del , CM000673.2:g.102789807del GRCh38
NC_000011.9:g.102660538del , CM000673.1:g.102660538del GRCh37
NC_000011.8:g.102165748del NCBI36
NG_011740.1:g.13431del
NG_011740.2:g.13431del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1195del (MMP1)
ENST00000681445.1:n.1191del (MMP1)
ENST00000681643.1:n.1217del (MMP1)
ENST00000371455.7:n.325-8217del (WTAPP1)
ENST00000525739.6:n.390-3338del (WTAPP1)
ENST00000544704.1:n.344+5743del (WTAPP1)
NR_038390.1:n.390-3338del (WTAPP1)