Canonical Allele Identifier: CA382209960
Gene: MMP7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.102398555G>C (hg19) chr11:g.102527824G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102527824G>C , CM000673.2:g.102527824G>C GRCh38
NC_000011.9:g.102398555G>C , CM000673.1:g.102398555G>C GRCh37
NC_000011.8:g.101903765G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260227.5:c.268C>G MANE Select ENSP00000260227.4:p.Pro90Ala
ENST00000260227.4:c.268C>G ENSP00000260227.4:p.Pro90Ala
ENST00000531200.1:n.315C>G
ENST00000533366.5:n.318C>G
NM_002423.3:c.268C>G NP_002414.1:p.Pro90Ala
NM_002423.4:c.268C>G NP_002414.1:p.Pro90Ala
NM_002423.5:c.268C>G MANE Select NP_002414.1:p.Pro90Ala
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