Canonical Allele Identifier: CA2615724339

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789788_102789793del , CM000673.2:g.102789788_102789793del GRCh38
NC_000011.9:g.102660519_102660524del , CM000673.1:g.102660519_102660524del GRCh37
NC_000011.8:g.102165729_102165734del NCBI36
NG_011740.1:g.13443_13448del
NG_011740.2:g.13443_13448del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1207_1212del (MMP1)
ENST00000681445.1:n.1203_1208del (MMP1)
ENST00000681643.1:n.1229_1234del (MMP1)
ENST00000371455.7:n.325-8236_325-8231del (WTAPP1)
ENST00000525739.6:n.390-3357_390-3352del (WTAPP1)
ENST00000544704.1:n.344+5724_344+5729del (WTAPP1)
NR_038390.1:n.390-3357_390-3352del (WTAPP1)