Canonical Allele Identifier: CA2615724434

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102789998C>A , CM000673.2:g.102789998C>A GRCh38
NC_000011.9:g.102660729C>A , CM000673.1:g.102660729C>A GRCh37
NC_000011.8:g.102165939C>A NCBI36
NG_011740.1:g.13238G>T
NG_011740.2:g.13238G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.*414G>T (MMP1) MANE Select ENSP00000322788.6:n.*414G>T
ENST00000680179.1:n.1002G>T (MMP1)
ENST00000681445.1:n.998G>T (MMP1)
ENST00000681643.1:n.1024G>T (MMP1)
ENST00000315274.6:c.*414G>T (MMP1) ENSP00000322788.6:n.*414G>T
ENST00000371455.7:n.325-8026C>A (WTAPP1)
ENST00000525739.6:n.390-3147C>A (WTAPP1)
ENST00000544704.1:n.344+5934C>A (WTAPP1)
NM_001145938.1:c.*414G>T (MMP1) NP_001139410.1:n.*414G>T
NM_002421.3:c.*414G>T (MMP1) NP_002412.1:n.*414G>T
NR_038390.1:n.390-3147C>A (WTAPP1)
NM_002421.4:c.*414G>T (MMP1) MANE Select NP_002412.1:n.*414G>T
NM_001145938.2:c.*414G>T (MMP1) NP_001139410.1:n.*414G>T