Canonical Allele Identifier: CA382208880

Gene: MMP7

Linked Data

• MyVariant Identifiers: chr11:g.102398393A>T (hg19) ; chr11:g.102527662A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527662A>T , CM000673.2:g.102527662A>T	GRCh38
NC_000011.9:g.102398393A>T , CM000673.1:g.102398393A>T	GRCh37
NC_000011.8:g.101903603A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.346T>A MANE Select	ENSP00000260227.4:p.Tyr116Asn
ENST00000260227.4:c.346T>A	ENSP00000260227.4:p.Tyr116Asn
ENST00000531200.1:n.393T>A
ENST00000533366.5:n.396T>A
NM_002423.3:c.346T>A	NP_002414.1:p.Tyr116Asn
NM_002423.4:c.346T>A	NP_002414.1:p.Tyr116Asn
NM_002423.5:c.346T>A MANE Select	NP_002414.1:p.Tyr116Asn