Canonical Allele Identifier: CA2724756976

Linked Data

dbSNP Id: rs2134359441

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789697del , CM000673.2:g.102789697del GRCh38
NC_000011.9:g.102660428del , CM000673.1:g.102660428del GRCh37
NC_000011.8:g.102165638del NCBI36
NG_011740.1:g.13542del
NG_011740.2:g.13542del

Transcript Alleles

HGVS Amino-acid Change
ENST00000680179.1:n.1306del (MMP1)
ENST00000681445.1:n.1302del (MMP1)
ENST00000681643.1:n.1328del (MMP1)
ENST00000371455.7:n.325-8327del (WTAPP1)
ENST00000525739.6:n.390-3448del (WTAPP1)
ENST00000544704.1:n.344+5633del (WTAPP1)
NR_038390.1:n.390-3448del (WTAPP1)