Canonical Allele Identifier: CA2581049915

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790228A= , CM000673.2:g.102790228A= GRCh38
NC_000011.9:g.102660959A= , CM000673.1:g.102660959A= GRCh37
NC_000011.8:g.102166169A= NCBI36
NG_011740.1:g.13008T=
NG_011740.2:g.13008T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*184T= (MMP1) MANE Select ENSP00000322788.6:n.*184T=
ENST00000680179.1:n.772T= (MMP1)
ENST00000681445.1:n.768T= (MMP1)
ENST00000681643.1:n.794T= (MMP1)
ENST00000315274.6:c.*184T= (MMP1) ENSP00000322788.6:n.*184T=
ENST00000371455.7:n.325-7796A= (WTAPP1)
ENST00000525739.6:n.390-2917A= (WTAPP1)
ENST00000544704.1:n.344+6164A= (WTAPP1)
NM_001145938.1:c.*184T= (MMP1) NP_001139410.1:n.*184T=
NM_002421.3:c.*184T= (MMP1) NP_002412.1:n.*184T=
NR_038390.1:n.390-2917A= (WTAPP1)
NM_002421.4:c.*184T= (MMP1) MANE Select NP_002412.1:n.*184T=
NM_001145938.2:c.*184T= (MMP1) NP_001139410.1:n.*184T=