Canonical Allele Identifier: CA382209563
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398509G>T (hg19) chr11:g.102527778G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527778G>T , CM000673.2:g.102527778G>T GRCh38
NC_000011.9:g.102398509G>T , CM000673.1:g.102398509G>T GRCh37
NC_000011.8:g.101903719G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.314C>A MANE Select ENSP00000260227.4:p.Thr105Asn
ENST00000260227.4:c.314C>A ENSP00000260227.4:p.Thr105Asn
ENST00000531200.1:n.361C>A
ENST00000533366.5:n.364C>A
NM_002423.3:c.314C>A NP_002414.1:p.Thr105Asn
NM_002423.4:c.314C>A NP_002414.1:p.Thr105Asn
NM_002423.5:c.314C>A MANE Select NP_002414.1:p.Thr105Asn
Search 100 bp 5'
Search 100 bp 3'