Canonical Allele Identifier: CA382209603
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398515T>A (hg19) chr11:g.102527784T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527784T>A , CM000673.2:g.102527784T>A GRCh38
NC_000011.9:g.102398515T>A , CM000673.1:g.102398515T>A GRCh37
NC_000011.8:g.101903725T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.308A>T MANE Select ENSP00000260227.4:p.Lys103Ile
ENST00000260227.4:c.308A>T ENSP00000260227.4:p.Lys103Ile
ENST00000531200.1:n.355A>T
ENST00000533366.5:n.358A>T
NM_002423.3:c.308A>T NP_002414.1:p.Lys103Ile
NM_002423.4:c.308A>T NP_002414.1:p.Lys103Ile
NM_002423.5:c.308A>T MANE Select NP_002414.1:p.Lys103Ile
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Search 100 bp 3'