Canonical Allele Identifier: CA2615724638

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790129_102790131del , CM000673.2:g.102790129_102790131del GRCh38
NC_000011.9:g.102660860_102660862del , CM000673.1:g.102660860_102660862del GRCh37
NC_000011.8:g.102166070_102166072del NCBI36
NG_011740.1:g.13105_13107del
NG_011740.2:g.13105_13107del

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*281_*283del (MMP1) MANE Select ENSP00000322788.6:n.*281_*283del
ENST00000680179.1:n.869_871del (MMP1)
ENST00000681445.1:n.865_867del (MMP1)
ENST00000681643.1:n.891_893del (MMP1)
ENST00000315274.6:c.*281_*283del (MMP1) ENSP00000322788.6:n.*281_*283del
ENST00000371455.7:n.325-7895_325-7893del (WTAPP1)
ENST00000525739.6:n.390-3016_390-3014del (WTAPP1)
ENST00000544704.1:n.344+6065_344+6067del (WTAPP1)
NM_001145938.1:c.*281_*283del (MMP1) NP_001139410.1:n.*281_*283del
NM_002421.3:c.*281_*283del (MMP1) NP_002412.1:n.*281_*283del
NR_038390.1:n.390-3016_390-3014del (WTAPP1)
NM_002421.4:c.*281_*283del (MMP1) MANE Select NP_002412.1:n.*281_*283del
NM_001145938.2:c.*281_*283del (MMP1) NP_001139410.1:n.*281_*283del