Canonical Allele Identifier: CA2497334475

Linked Data

dbSNP Id: rs1857968106

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789657_102789663del , CM000673.2:g.102789657_102789663del GRCh38
NC_000011.9:g.102660388_102660394del , CM000673.1:g.102660388_102660394del GRCh37
NC_000011.8:g.102165598_102165604del NCBI36
NG_011740.1:g.13575_13581del
NG_011740.2:g.13575_13581del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1339_1345del (MMP1)
ENST00000681445.1:n.1335_1341del (MMP1)
ENST00000681643.1:n.1361_1367del (MMP1)
ENST00000371455.7:n.325-8367_325-8361del (WTAPP1)
ENST00000525739.6:n.390-3488_390-3482del (WTAPP1)
ENST00000544704.1:n.344+5593_344+5599del (WTAPP1)
NR_038390.1:n.390-3488_390-3482del (WTAPP1)