Canonical Allele Identifier: CA382226734

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790739T>A , CM000673.2:g.102790739T>A GRCh38
NC_000011.9:g.102661470T>A , CM000673.1:g.102661470T>A GRCh37
NC_000011.8:g.102166680T>A NCBI36
NG_011740.1:g.12497A>T
NG_011740.2:g.12497A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1264A>T (MMP1) MANE Select ENSP00000322788.6:p.Ile422Phe
ENST00000680179.1:n.442A>T (MMP1)
ENST00000681445.1:n.438A>T (MMP1)
ENST00000681643.1:n.464A>T (MMP1)
ENST00000315274.6:c.1264A>T (MMP1) ENSP00000322788.6:p.Ile422Phe
ENST00000371455.7:n.325-7285T>A (WTAPP1)
ENST00000525739.6:n.390-2406T>A (WTAPP1)
ENST00000544704.1:n.344+6675T>A (WTAPP1)
NM_001145938.1:c.1066A>T (MMP1) NP_001139410.1:p.Ile356Phe
NM_002421.3:c.1264A>T (MMP1) NP_002412.1:p.Ile422Phe
NR_038390.1:n.390-2406T>A (WTAPP1)
NM_002421.4:c.1264A>T (MMP1) MANE Select NP_002412.1:p.Ile422Phe
NM_001145938.2:c.1066A>T (MMP1) NP_001139410.1:p.Ile356Phe