Canonical Allele Identifier: CA2615724378

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789880_102789882del , CM000673.2:g.102789880_102789882del GRCh38
NC_000011.9:g.102660611_102660613del , CM000673.1:g.102660611_102660613del GRCh37
NC_000011.8:g.102165821_102165823del NCBI36
NG_011740.1:g.13356_13358del
NG_011740.2:g.13356_13358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1120_1122del (MMP1)
ENST00000681445.1:n.1116_1118del (MMP1)
ENST00000681643.1:n.1142_1144del (MMP1)
ENST00000371455.7:n.325-8144_325-8142del (WTAPP1)
ENST00000525739.6:n.390-3265_390-3263del (WTAPP1)
ENST00000544704.1:n.344+5816_344+5818del (WTAPP1)
NR_038390.1:n.390-3265_390-3263del (WTAPP1)