Canonical Allele Identifier: CA2580582284
Community Standard Title: NM_002421.4(MMP1):c.315G= (p.Gly105=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102797291C= , CM000673.2:g.102797291C= GRCh38
NC_000011.9:g.102668022C= , CM000673.1:g.102668022C= GRCh37
NC_000011.8:g.102173232C= NCBI36
NG_011740.1:g.5945G=
NG_011740.2:g.5945G=

Transcript Alleles

HGVS Amino-acid Change
NM_002421.4:c.315G= (MMP1) MANE Select NP_002412.1:p.Gly105=
ENST00000315274.7:c.315G= (MMP1) MANE Select ENSP00000322788.6:p.Gly105=
NM_001145938.1:c.117G= (MMP1) NP_001139410.1:p.Gly39=
NM_001145938.2:c.117G= (MMP1) NP_001139410.1:p.Gly39=
NM_002421.3:c.315G= (MMP1) NP_002412.1:p.Gly105=
NR_038390.1:n.584-733C= (WTAPP1)
ENST00000315274.6:c.315G= (MMP1) ENSP00000322788.6:p.Gly105=
ENST00000371455.7:n.325-733C= (WTAPP1)
ENST00000525739.6:n.584-733C= (WTAPP1)
ENST00000544704.1:n.345-733C= (WTAPP1)