Canonical Allele Identifier: CA382208897

Gene: MMP7

Linked Data

• MyVariant Identifiers: chr11:g.102398402T>A (hg19) ; chr11:g.102527671T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527671T>A , CM000673.2:g.102527671T>A	GRCh38
NC_000011.9:g.102398402T>A , CM000673.1:g.102398402T>A	GRCh37
NC_000011.8:g.101903612T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.337A>T MANE Select	ENSP00000260227.4:p.Ile113Phe
ENST00000260227.4:c.337A>T	ENSP00000260227.4:p.Ile113Phe
ENST00000531200.1:n.384A>T
ENST00000533366.5:n.387A>T
NM_002423.3:c.337A>T	NP_002414.1:p.Ile113Phe
NM_002423.4:c.337A>T	NP_002414.1:p.Ile113Phe
NM_002423.5:c.337A>T MANE Select	NP_002414.1:p.Ile113Phe