Canonical Allele Identifier: CA382208889

Gene: MMP7

Linked Data

• MyVariant Identifiers: chr11:g.102398398A>T (hg19) ; chr11:g.102527667A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527667A>T , CM000673.2:g.102527667A>T	GRCh38
NC_000011.9:g.102398398A>T , CM000673.1:g.102398398A>T	GRCh37
NC_000011.8:g.101903608A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.341T>A MANE Select	ENSP00000260227.4:p.Val114Glu
ENST00000260227.4:c.341T>A	ENSP00000260227.4:p.Val114Glu
ENST00000531200.1:n.388T>A
ENST00000533366.5:n.391T>A
NM_002423.3:c.341T>A	NP_002414.1:p.Val114Glu
NM_002423.4:c.341T>A	NP_002414.1:p.Val114Glu
NM_002423.5:c.341T>A MANE Select	NP_002414.1:p.Val114Glu