Canonical Allele Identifier: CA2793420683

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789950C>A , CM000673.2:g.102789950C>A GRCh38
NC_000011.9:g.102660681C>A , CM000673.1:g.102660681C>A GRCh37
NC_000011.8:g.102165891C>A NCBI36
NG_011740.1:g.13286G>T
NG_011740.2:g.13286G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*462G>T (MMP1) MANE Select ENSP00000322788.6:n.*462G>T
ENST00000680179.1:n.1050G>T (MMP1)
ENST00000681445.1:n.1046G>T (MMP1)
ENST00000681643.1:n.1072G>T (MMP1)
ENST00000315274.6:c.*462G>T (MMP1) ENSP00000322788.6:n.*462G>T
ENST00000371455.7:n.325-8074C>A (WTAPP1)
ENST00000525739.6:n.390-3195C>A (WTAPP1)
ENST00000544704.1:n.344+5886C>A (WTAPP1)
NM_001145938.1:c.*462G>T (MMP1) NP_001139410.1:n.*462G>T
NM_002421.3:c.*462G>T (MMP1) NP_002412.1:n.*462G>T
NR_038390.1:n.390-3195C>A (WTAPP1)
NM_002421.4:c.*462G>T (MMP1) MANE Select NP_002412.1:n.*462G>T
NM_001145938.2:c.*462G>T (MMP1) NP_001139410.1:n.*462G>T