Canonical Allele Identifier: CA2615724691

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790142_102790143insA , CM000673.2:g.102790142_102790143insA GRCh38
NC_000011.9:g.102660873_102660874insA , CM000673.1:g.102660873_102660874insA GRCh37
NC_000011.8:g.102166083_102166084insA NCBI36
NG_011740.1:g.13093_13094insT
NG_011740.2:g.13093_13094insT

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*269_*270insT (MMP1) MANE Select ENSP00000322788.6:n.*269_*270insT
ENST00000680179.1:n.857_858insT (MMP1)
ENST00000681445.1:n.853_854insT (MMP1)
ENST00000681643.1:n.879_880insT (MMP1)
ENST00000315274.6:c.*269_*270insT (MMP1) ENSP00000322788.6:n.*269_*270insT
ENST00000371455.7:n.325-7882_325-7881insA (WTAPP1)
ENST00000525739.6:n.390-3003_390-3002insA (WTAPP1)
ENST00000544704.1:n.344+6078_344+6079insA (WTAPP1)
NM_001145938.1:c.*269_*270insT (MMP1) NP_001139410.1:n.*269_*270insT
NM_002421.3:c.*269_*270insT (MMP1) NP_002412.1:n.*269_*270insT
NR_038390.1:n.390-3003_390-3002insA (WTAPP1)
NM_002421.4:c.*269_*270insT (MMP1) MANE Select NP_002412.1:n.*269_*270insT
NM_001145938.2:c.*269_*270insT (MMP1) NP_001139410.1:n.*269_*270insT